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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YBL051C PIN4 / SGDID:S000000147
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
Yeast Systematic Name Yeast Symbol SGDID Analog Name Analog Description EC Organism Disease Structure Uniprot Human ID Human Symbol HHsearch Probability HHsearch E_value HHsearch P_value HHsearch Score Flag Disease related Flag Homo sapiens Flag Mus musculus Flag Danio rerio Flag Drosophila melanogaster Flag Caenorhabditis elegans Flag Arabidopsis thaliana Flag Escherichia coli
YBL051C PIN4 SGDID:S000000147
HNRNPD AUF1 HNRPD
Heterogeneous nuclear ribonucleoprotein D0 (hnRNP D0) (AU-rich element RNA-binding protein 1)
Homo sapiens
Follicular Adenoma,Ulcerative Blepharitis,Chromosome 4q21 Deletion Syndrome
1x0f_a Q14103 ENSG00000138668 HNRNPD 96.50 6.70E-06 9.90E-10 54.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Pabpn1l-b epabp2-b pabpnl1-b
Embryonic polyadenylate-binding protein 2-B (Embryonic poly(A)-binding protein 2-B) (XePABP2-B) (ePABP-2B) (ePABP2-B) (Embryonic poly(A)-binding protein type II-B)
Xenopus laevis
2jwn_b Q6TY21 96.70 3.00E-06 4.00E-10 64.50 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PSPC1 PSP1
Paraspeckle component 1 (Paraspeckle protein 1)
Homo sapiens
Fanconi Anemia, Complementation Group A
3sde_a Q8WXF1 ENSG00000121390 PSPC1 96.20 1.50E-05 2.00E-09 68.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNRPA
SNRPA
Oryctolagus cuniculus
6cmn_a G1TM83 97.00 9.50E-07 1.10E-10 70.70 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SRSF8 SFRS2B SRP46
Serine/arginine-rich splicing factor 8 (Pre-mRNA-splicing factor SRP46) (Splicing factor SRp46) (Splicing factor, arginine/serine-rich 2B)
Homo sapiens
2dnm_a Q9BRL6 ENSG00000263465 SRSF8 96.60 4.50E-06 6.60E-10 58.90 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1
U1 small nuclear ribonucleoprotein 70 kDa (U1 snRNP 70 kDa) (U1-70K) (snRNP70)
Homo sapiens
Systemic Scleroderma,Facial Hemiatrophy,Dyskinesia Of Esophagus,Connective Tissue Disease,Splenic Tuberculosis,Telangiectasis,Collagen Disease,Lupus Erythematosus,Childhood Type Dermatomyositis,Mixed Connective Tissue Disease,Limited Scleroderma,Diffuse Scleroderma,Raynaud Disease,Heart Block, Congenital,Hypotrichosis 13,Pericardium Disease,Autoimmune Disease Of Exocrine System,Crest Syndrome,Systemic Lupus Erythematosus,Syndromic X-Linked Intellectual Disability Cabezas Type
6qx9_1k P08621 ENSG00000104852 SNRNP70 96.20 2.30E-05 2.60E-09 75.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Eif4h Wbscr1
Eukaryotic translation initiation factor 4H (eIF-4H) (Williams-Beuren syndrome chromosomal region 1 protein homolog)
Mus musculus
2dng_a Q9WUK2 96.50 6.00E-06 8.40E-10 59.80 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PUB1 RNP1 YNL016W N2842
Nuclear and cytoplasmic polyadenylated RNA-binding protein PUB1 (ARS consensus-binding protein ACBP-60) (Poly uridylate-binding protein) (Poly(U)-binding protein)
Saccharomyces cerevisiae
2la4_a P32588 96.50 6.30E-06 8.80E-10 59.40 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SYF2 NTC31 YGR129W
Pre-mRNA-splicing factor SYF2 (PRP19 complex protein 31) (Synthetic lethal with CDC40 protein 2)
Saccharomyces cerevisiae
6exn_y P53277 96.60 4.10E-06 5.40E-10 63.60 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NAM8 MRE2 YHR086W
Protein NAM8
Saccharomyces cerevisiae
5zwn_v Q00539 96.20 2.00E-05 2.40E-09 76.90 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ELAVL1 HUR
ELAV-like protein 1 (Hu-antigen R) (HuR)
Homo sapiens
Follicular Adenoma,Retinitis Pigmentosa,Myopathy,Myotonic Dystrophy 1,Cervical Non-Keratinizing Squamous Cell Carcinoma,Periampullary Adenocarcinoma,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Juvenile Polyposis Syndrome,Disease Of Mental Health,Retinitis Pigmentosa 49,Scalp-Ear-Nipple Syndrome,Renal Cell Carcinoma, Nonpapillary
5szw_a Q15717 ENSG00000066044 ELAVL1 96.20 1.80E-05 2.70E-09 55.40 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PF3D7_0517300
PF3D7_0517300
Plasmodium falciparum
2n7c_a Q8I3T5 96.00 2.70E-05 4.10E-09 52.60 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM41
RNA-binding protein 41 (RNA-binding motif protein 41)
Homo sapiens
2cpx_a Q96IZ5 ENSG00000089682 RBM41 97.00 5.90E-07 8.10E-11 66.90 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SPBC56F2.08c
Pumilio domain-containing protein C56F2.08c
Schizosaccharomyces pombe
6nx5_a O60059 95.90 3.70E-05 5.40E-09 51.70 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM22 ZC3H16 199G4
Pre-mRNA-splicing factor RBM22 (RNA-binding motif protein 22) (Zinc finger CCCH domain-containing protein 16)
Homo sapiens
2ytc_a Q9NW64 ENSG00000086589 RBM22 95.90 3.50E-05 5.00E-09 52.50 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
EIF4B
Eukaryotic translation initiation factor 4B (eIF-4B)
Homo sapiens
Mouth Disease
2j76_e P23588 ENSG00000063046 EIF4B 96.10 2.20E-05 2.80E-09 59.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PES4 YFR023W
Protein PES4 (DNA polymerase epsilon suppressor 4)
Saccharomyces cerevisiae
6exx_a P39684 96.50 5.70E-06 8.40E-10 55.20 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
TARDBP TDP43
TAR DNA-binding protein 43 (TDP-43)
Homo sapiens
Supranuclear Palsy, Progressive, 1,Mutism,Myopathy,Amyotrophic Lateral Sclerosis 11,Akinetic Mutism,Myofibrillar Myopathy,Neuromuscular Disease,Alzheimer Disease,Pica Disease,Dysgraphia,Nominal Aphasia,Amyotrophic Lateral Sclerosis 1,Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Ideomotor Apraxia,Giant Axonal Neuropathy 2,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Movement Disease,Muscular Atrophy,Dyscalculia,Distal Hereditary Motor Neuronopathy Type 7,Pseudobulbar Palsy,Locked-In Syndrome,Prosopagnosia,Machado-Joseph Disease,Arteriolosclerosis,Multisystem Proteinopathy,Semantic Dementia,Dementia,Tardbp-Related Amyotrophic Lateral Sclerosis,Alexia,Amyotrophic Lateral Sclerosis 4, Juvenile,Perry Syndrome,Speech And Communication Disorders,Progressive Muscular Atrophy,Pick Disease Of Brain,Postencephalitic Parkinson Disease,Autosomal Dominant Cerebellar Ataxia,Amyotrophic Lateral Sclerosis 19,Niemann-Pick Disease,Liposarcoma,Disease Of Mental Health,Masp2 Deficiency,Dermatopathia Pigmentosa Reticularis,Dementia, Lewy Body,Fragile X Syndrome,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Ophthalmomyiasis,Spinocerebellar Ataxia 2,Nonaka Myopathy,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4,Huntington Disease,Epilepsy, Idiopathic Generalized 2,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Aphasia,Writing Disorder,Inclusion Body Myositis,Associative Agnosia,Simultanagnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 12,Agraphia,Neuronopathy, Distal Hereditary Motor, Type Viib,Amyotrophic Lateral Sclerosis, Juvenile, With Dementia,Amyotrophic Lateral Sclerosis Type 22,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7
2cqg_a Q13148 ENSG00000120948 TARDBP 95.90 3.70E-05 5.80E-09 51.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Msi1 Msi1h
RNA-binding protein Musashi homolog 1 (Musashi-1)
Mus musculus
2mst_a Q61474 96.40 9.00E-06 1.40E-09 51.70 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
gw GW182 CG31992
Protein Gawky
Drosophila melanogaster
2wbr_a Q8SY33 96.60 4.90E-06 6.70E-10 59.30 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
Hnrnpl Fblim1
Heterogeneous nuclear ribonucleoprotein L (hnRNP L)
Rattus norvegicus
2mqn_a F1LQ48 96.60 3.30E-06 4.80E-10 67.40 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Nono
Non-POU domain-containing octamer-binding protein (NonO protein)
Mus musculus
2cpj_a Q99K48 96.10 2.60E-05 3.70E-09 55.60 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NCL
Nucleolin (Protein C23)
Mesocricetus auratus
1fj7_a P08199 96.40 8.10E-06 1.10E-09 59.80 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
tsu Y14 CG8781
RNA-binding protein 8A (Protein tsunagi)
Drosophila melanogaster
1oo0_b Q9V535 96.30 1.20E-05 1.70E-09 58.00 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
TIA1
Nucleolysin TIA-1 isoform p40 (RNA-binding protein TIA-1) (T-cell-restricted intracellular antigen-1) (TIA-1) (p40-TIA-1)
Homo sapiens
Gastrointestinal Lymphoma,Lymphomatoid Granulomatosis,Lymphomatoid Papulosis,Lethal Midline Granuloma,Viral Esophagitis,Myopathy,B-Cell Lymphoma,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Motor Neuron Disease,Orbit Lymphoma,Rhinosporidiosis,Angioimmunoblastic T-Cell Lymphoma,Leber Plus Disease,Amyotrophic Lateral Sclerosis 26 With Or Without Frontotemporal Dementia,Multisystem Proteinopathy,Dementia,Breast Lipoma,Reticulosarcoma,Sezary'S Disease,Aggressive Nk-Cell Leukemia,T-Cell Adult Acute Lymphocytic Leukemia,Giardiasis,Composite Lymphoma,Pediatric Lymphoma,Nasal Cavity Lymphoma,Primary Cutaneous Anaplastic Large Cell Lymphoma,Hepatosplenic T-Cell Lymphoma,Disease Of Mental Health,Panniculitis,Skin Disease,Welander Distal Myopathy,Erythema Multiforme,Lymphoma, Hodgkin, Classic,Lymphocytic Gastritis,Parasitic Ichthyosporea Infectious Disease,Mature T-Cell And Nk-Cell Lymphoma,Anaplastic Large Cell Lymphoma,Peripheral T-Cell Lymphoma,Lymphoma,Cutaneous T Cell Lymphoma,Lichen Sclerosus Et Atrophicus,Mycosis Fungoides,Lymphoproliferative Syndrome,Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood,Frontotemporal Dementia,Celiac Disease 1
3bs9_a P31483 ENSG00000116001 TIA1 96.50 5.80E-06 9.00E-10 54.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NCBP2 CBP20 PIG55
Nuclear cap-binding protein subunit 2 (20 kDa nuclear cap-binding protein) (Cell proliferation-inducing gene 55 protein) (NCBP 20 kDa subunit) (CBP20) (NCBP-interacting protein 1) (NIP1)
Homo sapiens
Chromosome 22q11.2 Deletion Syndrome, Distal
1h6k_z P52298 ENSG00000114503 NCBP2 96.20 1.80E-05 2.60E-09 55.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SF3B4 SAP49
Splicing factor 3B subunit 4 (Pre-mRNA-splicing factor SF3b 49 kDa subunit) (Spliceosome-associated protein 49) (SAP 49)
Homo sapiens
Dysostosis,Synostosis,Burn-Mckeown Syndrome,Phocomelia,Radioulnar Synostosis,Charcot-Marie-Tooth Disease X-Linked Recessive 4,Hereditary Hearing Loss And Deafness,Usher Syndrome, Type Iia,Cerebrocostomandibular Syndrome,Cleft Palate, Isolated,Mandibulofacial Dysostosis, Guion-Almeida Type,Ehlers-Danlos Syndrome, Classic Type, 1,Humeroradial Synostosis,Acrofacial Dysostosis Syndrome Of Rodriguez,Acrofacial Dysostosis,Acrofacial Dysostosis 1, Nager Type,Treacher Collins Syndrome 1,Postaxial Acrofacial Dysostosis
1x5t_a Q15427 ENSG00000143368 SF3B4 96.60 4.40E-06 6.60E-10 57.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ALYREF ALY BEF THOC4
THO complex subunit 4 (Tho4) (Ally of AML-1 and LEF-1) (Aly/REF export factor) (Transcriptional coactivator Aly/REF) (bZIP-enhancing factor BEF)
Homo sapiens
Sarcoma,Dermatopathia Pigmentosa Reticularis,Systemic Lupus Erythematosus
3ulh_a Q86V81 ENSG00000183684 ALYREF 96.10 2.50E-05 3.40E-09 56.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
MSI2
RNA-binding protein Musashi homolog 2 (Musashi-2)
Homo sapiens
Colon Small Cell Carcinoma,Pineal Region Germinoma,B-Cell Adult Acute Lymphocytic Leukemia
6dbp_b Q96DH6 ENSG00000153944 MSI2 96.30 1.30E-05 1.90E-09 54.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
bru1 aret bruno CG31762
bru1 aret bruno CG31762
Drosophila melanogaster
2khc_a O18409 96.20 1.80E-05 2.40E-09 59.70 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
Alyref2 Ref2 Refbp2
Aly/REF export factor 2 (Alyref) (RNA and export factor-binding protein 2)
Mus musculus
2yka_a Q9JJW6 96.20 1.70E-05 2.30E-09 60.90 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Sxl Sx1 CG43770
Protein sex-lethal
Drosophila melanogaster
2sxl_a P19339 96.90 1.30E-06 2.00E-10 58.40 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM8A RBM8 HSPC114 MDS014
RNA-binding protein 8A (Binder of OVCA1-1) (BOV-1) (RNA-binding motif protein 8A) (RNA-binding protein Y14) (Ribonucleoprotein RBM8A)
Homo sapiens
Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Blood Platelet Disease,Endometrial Mixed Adenocarcinoma,Blood Coagulation Disease,Orofaciodigital Syndrome X,Thrombocytopenia-Absent Radius Syndrome,Thoracic Outlet Syndrome,Usher Syndrome, Type I,Microcephaly,Pick Disease Of Brain,Disease Of Mental Health,Thrombocytopenia,Amegakaryocytic Thrombocytopenia, Congenital,Dystonia 16,Holt-Oram Syndrome,Cardiomyopathy, Dilated, 1m
1p27_d Q9Y5S9 ENSG00000265241 RBM8A 96.20 1.60E-05 2.30E-09 57.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
HRB1 TOM34 YNL004W N2009
Protein HRB1 (Protein TOM34)
Saccharomyces cerevisiae
2mzr_a P38922 95.80 4.80E-05 6.90E-09 53.00 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
cwf2 prp3 SPAC3A12.11c
Pre-mRNA-splicing factor cwf2 (Complexed with cdc5 protein 2) (Pre-mRNA-processing protein 3)
Schizosaccharomyces pombe
3jb9_y P87126 96.20 2.30E-05 2.50E-09 76.10 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
LSM6 YDR378C D9481.18
U6 snRNA-associated Sm-like protein LSm6
Saccharomyces cerevisiae
5zwm_x Q06406 97.30 1.60E-07 2.10E-11 75.50 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
GNPTAB GNPTA KIAA1208
N-acetylglucosamine-1-phosphotransferase subunits alpha/beta (EC 2.7.8.17) (GlcNAc-1-phosphotransferase subunits alpha/beta) (Stealth protein GNPTAB) (UDP-N-acetylglucosamine-1-phosphotransferase subunits alpha/beta) [Cleaved into: N-acetylglucosamine-1-phosphotransferase subunit alpha; N-acetylglucosamine-1-phosphotransferase subunit beta]
2.7.8.17 Homo sapiens
Articulation Disorder,Speech Disorder,Mucolipidosis,Tibial Neuropathy,Dyslexia,Tarsal Tunnel Syndrome,Vestibulocochlear Nerve Disease,Vestibular Neuronitis,Osteochondrosis,Mucopolysaccharidosis Iii,Mucopolysaccharidosis-Plus Syndrome,Gnptab-Related Disorders,Gm2-Gangliosidosis, Ab Variant,Gingival Hypertrophy,Disseminated Chorioretinitis,Benign Essential Hypertension,Mucolipidoses,Deficiency Anemia,46,Xy Sex Reversal 7,Osteogenesis Imperfecta, Type Vii,Scheuermann Disease,Autosomal Recessive Disease,Hurler Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2v,Her2-Receptor Positive Breast Cancer,Stuttering,Legg-Calve-Perthes Disease,Mucolipidosis Ii Alpha/Beta,Mucolipidosis Iii Alpha/Beta,Mucolipidosis Iii Gamma,Mucopolysaccharidosis, Type Iiia
2n6d_a Q3T906 ENSG00000111670 GNPTAB 96.50 7.50E-06 9.00E-10 68.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Rbm19
Probable RNA-binding protein 19 (RNA-binding motif protein 19)
Mus musculus
2cpf_a Q8R3C6 96.10 1.90E-05 2.90E-09 54.10 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RGP-1a LOC107800679
RGP-1a LOC107800679
Nicotiana tabacum
4c7q_a D6PZY5 96.20 1.70E-05 2.80E-09 51.00 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
HSH49 YOR319W O6142
Protein HSH49
Saccharomyces cerevisiae
5lsl_d Q99181 96.40 1.00E-05 1.40E-09 58.00 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PAB1 YER165W
Polyadenylate-binding protein, cytoplasmic and nuclear (PABP) (Poly(A)-binding protein) (ARS consensus-binding protein ACBP-67) (Polyadenylate tail-binding protein)
Saccharomyces cerevisiae
6r5k_h P04147 96.80 2.20E-06 3.00E-10 82.00 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ACIN1 ACINUS KIAA0670
Apoptotic chromatin condensation inducer in the nucleus (Acinus)
Homo sapiens
Breast Adenomyoepithelioma,Large Cell Acanthoma,Pilar Sheath Acanthoma,Breast Myoepithelial Neoplasm,Angioma Serpiginosum,Desmoid Disease, Hereditary
6g6s_a Q9UKV3 ENSG00000100813 ACIN1 96.30 1.30E-05 1.90E-09 55.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PTBP1 PTB
Polypyrimidine tract-binding protein 1 (PTB) (57 kDa RNA-binding protein PPTB-1) (Heterogeneous nuclear ribonucleoprotein I) (hnRNP I)
Homo sapiens
Endometrial Stromal Sarcoma,Myopathy,Bulbar Polio,Atrial Septal Defect 1,Human T-Cell Leukemia Virus Type 2,Patellar Tendinitis,Congenital Myasthenic Syndrome,Mouth Disease,Paralytic Poliomyelitis,Atrial Septal Defect 2,Frontotemporal Dementia
1qm9_a P26599 ENSG00000011304 PTBP1 96.60 3.60E-06 5.30E-10 65.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PRP24 YMR268C YM8156.10C
U4/U6 snRNA-associated-splicing factor PRP24 (U4/U6 snRNP protein)
Saccharomyces cerevisiae
2go9_a P49960 96.40 7.10E-06 1.00E-09 62.10 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NONO NRB54
Non-POU domain-containing octamer-binding protein (NonO protein) (54 kDa nuclear RNA- and DNA-binding protein) (55 kDa nuclear protein) (DNA-binding p52/p100 complex, 52 kDa subunit) (NMT55) (p54(nrb)) (p54nrb)
Homo sapiens
Heart Disease,Small Intestine Neuroendocrine Neoplasm,Small Intestine Benign Neoplasm,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Xp11-Associated,Mental Retardation, X-Linked, Syndromic 34,Syndromic Intellectual Disability
5ifm_j Q15233 ENSG00000147140 NONO 97.20 2.20E-07 2.80E-11 80.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM23 RNPC4 PP239
Probable RNA-binding protein 23 (CAPER beta) (CAPERbeta) (RNA-binding motif protein 23) (RNA-binding region-containing protein 4) (Splicing factor SF2)
Homo sapiens
2cq4_a Q86U06 ENSG00000100461 RBM23 96.70 3.50E-06 4.70E-10 63.20 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBPMS HERMES
RNA-binding protein with multiple splicing (RBP-MS) (Heart and RRM expressed sequence) (Hermes)
Homo sapiens
Optic Nerve Disease,Ocular Hypertension,Hordeolum,Retinal Ischemia,Optic Nerve Hypoplasia, Bilateral
5cyj_b Q93062 96.80 1.60E-06 2.10E-10 63.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
IGF2BP3 IMP3 KOC1 VICKZ3
Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2 mRNA-binding protein 3) (IMP-3) (IGF-II mRNA-binding protein 3) (KH domain-containing protein overexpressed in cancer) (hKOC) (VICKZ family member 3)
Homo sapiens
Enchondroma,Pilomyxoid Astrocytoma,Pilocytic Astrocytoma,Adenocarcinoma In Situ,Pancreatic Cancer
6fq1_a O00425 ENSG00000136231 IGF2BP3 96.00 3.10E-05 4.30E-09 60.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CPEB1 CPEB
Cytoplasmic polyadenylation element-binding protein 1 (CPE-BP1) (CPE-binding protein 1) (h-CPEB) (hCPEB-1)
Homo sapiens
Diamond-Blackfan Anemia 4,Premature Menopause,Disease Of Mental Health,Scalp-Ear-Nipple Syndrome,Fragile X Syndrome
2mkk_a Q9BZB8 ENSG00000214575 CPEB1 96.50 6.60E-06 9.80E-10 64.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
HNRNPA1 HNRPA1
Heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) (Helix-destabilizing protein) (Single-strand RNA-binding protein) (hnRNP core protein A1) [Cleaved into: Heterogeneous nuclear ribonucleoprotein A1, N-terminally processed]
Homo sapiens
Lattice Corneal Dystrophy,Endometrial Stromal Sarcoma,Myopathy,Amyotrophic Lateral Sclerosis 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Autosomal Dominant Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Muscular Atrophy,Relapsing-Remitting Multiple Sclerosis,Atrial Septal Defect 1,Human T-Cell Leukemia Virus Type 2,Endometrial Stromal Tumor,Oculopharyngeal Muscular Dystrophy,Multisystem Proteinopathy,Dementia,Paget'S Disease Of Bone,Burkitt Lymphoma,Colorectal Cancer,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3,Amyotrophic Lateral Sclerosis 20,Disease Of Mental Health,Dermatopathia Pigmentosa Reticularis,Multiple Sclerosis,Spinocerebellar Ataxia 2,Immune Deficiency Disease,Secondary Progressive Multiple Sclerosis,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Inflammatory Myofibroblastic Tumor,Epithelial-Stromal Tgfbi Dystrophy,Frontotemporal Dementia
1l3k_a P09651 ENSG00000135486 HNRNPA1 97.20 3.00E-07 4.40E-11 72.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM19 KIAA0682
Probable RNA-binding protein 19 (RNA-binding motif protein 19)
Homo sapiens
Diamond-Blackfan Anemia,Ulnar-Mammary Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Autosomal Dominant Non-Syndromic Intellectual Disability 1
2dgw_a Q9Y4C8 ENSG00000122965 RBM19 96.80 2.10E-06 2.70E-10 63.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBMX HNRPG RBMXP1
RNA-binding motif protein, X chromosome (Glycoprotein p43) (Heterogeneous nuclear ribonucleoprotein G) (hnRNP G) [Cleaved into: RNA-binding motif protein, X chromosome, N-terminally processed]
Homo sapiens
Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Syndromic X-Linked Intellectual Disability,Syndromic X-Linked Intellectual Disability Shashi Type
2mb0_b P38159 ENSG00000147274 RBMX 96.50 6.10E-06 9.60E-10 55.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
TRA2B SFRS10
Transformer-2 protein homolog beta (TRA-2 beta) (TRA2-beta) (hTRA2-beta) (Splicing factor, arginine/serine-rich 10) (Transformer-2 protein homolog B)
Homo sapiens
Endometrial Stromal Sarcoma,Spinal Muscular Atrophy,Muscular Atrophy,Endometrial Stromal Tumor,Frontotemporal Dementia
2cqc_a P62995 ENSG00000136527 TRA2B 96.00 2.60E-05 4.10E-09 51.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SRSF2 SFRS2
Serine/arginine-rich splicing factor 2 (Protein PR264) (Splicing component, 35 kDa) (Splicing factor SC35) (SC-35) (Splicing factor, arginine/serine-rich 2)
Homo sapiens
Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Patau Syndrome,Amyotrophic Lateral Sclerosis 1,Extracutaneous Mastocytoma,Indolent Systemic Mastocytosis,Spinal Muscular Atrophy,Sm-Ahnmd,Aggressive Systemic Mastocytosis,Leukemia, Acute Myeloid,Systemic Mastocytosis With Associated Hematologic Neoplasm,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Dilated Cardiomyopathy,Endometrial Stromal Tumor,Acute Megakaryoblastic Leukemia In Down Syndrome,Chronic Leukemia,Systemic Mastocytosis,Mastocytosis,Lactic Acidosis,Immune Deficiency Disease,Myelodysplastic Syndrome,Down Syndrome,Holt-Oram Syndrome,Myelofibrosis,Atypical Chronic Myeloid Leukemia,Melanoma, Uveal
2kn4_a Q01130 ENSG00000161547 SRSF2 96.20 1.70E-05 2.50E-09 60.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CPEB4 KIAA1673
Cytoplasmic polyadenylation element-binding protein 4 (CPE-BP4) (CPE-binding protein 4) (hCPEB-4)
Homo sapiens
2mki_a Q17RY0 ENSG00000113742 CPEB4 96.40 8.80E-06 1.30E-09 64.20 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CELF5 BRUNOL5
CUGBP Elav-like family member 5 (CELF-5) (Bruno-like protein 5) (CUG-BP- and ETR-3-like factor 5) (RNA-binding protein BRUNOL-5)
Homo sapiens
Familial Febrile Seizures,Atrial Septal Defect 1,Specific Language Impairment
2dnh_a Q8N6W0 ENSG00000161082 CELF5 96.50 6.90E-06 9.60E-10 59.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
nono-1 CELE_F25B5.7 F25B5.7
nono-1 CELE_F25B5.7 F25B5.7
Caenorhabditis elegans
5ca5_a B3GWA1 96.90 1.10E-06 1.40E-10 75.90 0 0 0 0 0 1 0 0
YBL051C PIN4 SGDID:S000000147
RBM14 SIP
RNA-binding protein 14 (Paraspeckle protein 2) (PSP2) (RNA-binding motif protein 14) (RRM-containing coactivator activator/modulator) (Synaptotagmin-interacting protein) (SYT-interacting protein)
Homo sapiens
Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy
2dnp_a Q96PK6 ENSG00000248643 RBM14-RBM4 96.40 9.10E-06 1.30E-09 56.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CELF2 BRUNOL3 CUGBP2 ETR3 NAPOR
CUGBP Elav-like family member 2 (CELF-2) (Bruno-like protein 3) (CUG triplet repeat RNA-binding protein 2) (CUG-BP2) (CUG-BP- and ETR-3-like factor 2) (ELAV-type RNA-binding protein 3) (ETR-3) (Neuroblastoma apoptosis-related RNA-binding protein) (hNAPOR) (RNA-binding protein BRUNOL-3)
Homo sapiens
Childhood Absence Epilepsy,Ischemic Neuropathy,Myotonic Disease,Myotonic Dystrophy 1,Neuroblastoma,Spinal And Bulbar Muscular Atrophy, X-Linked 1
4tlq_a O95319 ENSG00000048740 CELF2 96.70 2.30E-06 3.40E-10 58.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PUF60 FIR ROBPI SIAHBP1
Poly(U)-binding-splicing factor PUF60 (60 kDa poly(U)-binding-splicing factor) (FUSE-binding protein-interacting repressor) (FBP-interacting repressor) (Ro-binding protein 1) (RoBP1) (Siah-binding protein 1) (Siah-BP1)
Homo sapiens
Charge Syndrome,Thymus Lymphoma,Microcephaly,Coloboma Of Macula,Verheij Syndrome,Xeroderma Pigmentosum, Complementation Group B,Neurodevelopmental Disorder With Hypotonia And Variable Intellectual And Behavioral Abnormalities
2kxf_a Q9UHX1 ENSG00000179950 PUF60 96.90 9.10E-07 1.40E-10 69.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
U2AF2 U2AF65
Splicing factor U2AF 65 kDa subunit (U2 auxiliary factor 65 kDa subunit) (hU2AF(65)) (hU2AF65) (U2 snRNP auxiliary factor large subunit)
Homo sapiens
Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Spinocerebellar Ataxia 1,Frontotemporal Dementia
2hzc_a P26368 ENSG00000063244 U2AF2 96.30 1.30E-05 1.70E-09 57.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
MSL1 YIR009W YIB9W
U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'')
Saccharomyces cerevisiae
6j6g_a P40567 96.50 6.30E-06 8.10E-10 62.80 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM39 HCC1 RNPC2
RNA-binding protein 39 (CAPER alpha) (CAPERalpha) (Hepatocellular carcinoma protein 1) (RNA-binding motif protein 39) (RNA-binding region-containing protein 2) (Splicing factor HCC1)
Homo sapiens
Hepatocellular Carcinoma
2jrs_a Q14498 ENSG00000131051 RBM39 96.10 2.40E-05 3.20E-09 58.40 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBPMS2
RNA-binding protein with multiple splicing 2 (RNA binding protein, mRNA processing factor 2)
Homo sapiens
Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome
2m9k_a Q6ZRY4 ENSG00000166831 RBPMS2 96.60 4.80E-06 6.60E-10 59.50 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
TAF15 RBP56 TAF2N
TATA-binding protein-associated factor 2N (68 kDa TATA-binding protein-associated factor) (TAF(II)68) (TAFII68) (RNA-binding protein 56)
Homo sapiens
Chondrosarcoma,Extraskeletal Mesenchymal Chondrosarcoma,Extraosseous Chondrosarcoma,Amyotrophic Lateral Sclerosis 1,Acute Leukemia,Intracranial Chondrosarcoma,Multisystem Proteinopathy,Lung Sarcoma,Myxoid Chondrosarcoma,Liposarcoma,Ewing Sarcoma,Chondrosarcoma, Extraskeletal Myxoid,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4,Bone Chondrosarcoma
2mmy_a Q92804 ENSG00000270647 TAF15 96.50 6.30E-06 8.60E-10 60.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
mec-8 CELE_F46A9.6 F46A9.6
mec-8 CELE_F46A9.6 F46A9.6
Caenorhabditis elegans
5tkz_b G5ECJ4 96.80 2.10E-06 3.00E-10 61.30 0 0 0 0 0 1 0 0
YBL051C PIN4 SGDID:S000000147
LARP6
La-related protein 6 (Acheron) (Achn) (La ribonucleoprotein domain family member 6)
Homo sapiens
Brittle Bone Disorder
2mtg_a Q9BRS8 ENSG00000166173 LARP6 96.80 2.00E-06 2.20E-10 71.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNRPA
U1 small nuclear ribonucleoprotein A (U1 snRNP A) (U1-A) (U1A)
Homo sapiens
Connective Tissue Disease,Autoimmune Disease,Neuropathy, Hereditary Sensory And Autonomic, Type Iib,Mixed Connective Tissue Disease,Syndromic Intellectual Disability,Neuropathy, Hereditary Sensory And Autonomic, Type Iia
1nu4_b P09012 ENSG00000077312 SNRPA 96.50 5.90E-06 8.30E-10 59.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBMX2 CGI-79
RNA-binding motif protein, X-linked 2
Homo sapiens
Theileriasis,Spermatogenic Failure, X-Linked, 1
6ff7_1 Q9Y388 ENSG00000134597 RBMX2 96.10 2.70E-05 3.40E-09 70.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
MUD1 YBR119W YBR0915
U1 small nuclear ribonucleoprotein A (U1 snRNP A) (U1-A) (U1A) (Mutant U1 die protein 1)
Saccharomyces cerevisiae
5zwn_s P32605 96.10 2.70E-05 3.60E-09 68.30 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NOP15 YNL110C N1954
Ribosome biogenesis protein 15 (Nucleolar protein 15)
Saccharomyces cerevisiae
5t9p_a P53927 96.90 1.20E-06 1.70E-10 65.00 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNP1 YIL061C
U1 small nuclear ribonucleoprotein 70 kDa homolog (U1 70K) (U1 snRNP 70 kDa homolog) (U1-70K) (U1 small nuclear ribonucleoprotein SNP1) (U1 snRNP protein SNP1)
Saccharomyces cerevisiae
5zwn_q Q00916 96.50 7.10E-06 8.60E-10 74.40 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SRSF7 SFRS7
Serine/arginine-rich splicing factor 7 (Splicing factor 9G8) (Splicing factor, arginine/serine-rich 7)
Homo sapiens
Frontotemporal Dementia
2hvz_a Q16629 ENSG00000115875 SRSF7 96.40 7.50E-06 1.10E-09 58.50 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RAVER1 KIAA1978
Ribonucleoprotein PTB-binding 1 (Protein raver-1)
Homo sapiens
3h2v_e Q8IY67 ENSG00000161847 RAVER1 96.00 2.60E-05 3.80E-09 52.10 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM47
RNA-binding protein 47 (RNA-binding motif protein 47)
Homo sapiens
Lung Acinar Adenocarcinoma
2dis_a A0AV96 ENSG00000163694 RBM47 96.10 2.00E-05 3.20E-09 53.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CELF6 BRUNOL6
CUGBP Elav-like family member 6 (CELF-6) (Bruno-like protein 6) (CUG-BP- and ETR-3-like factor 6) (RNA-binding protein BRUNOL-6)
Homo sapiens
Atrial Septal Defect 1,Optic Nerve Neoplasm,Autism
2dgq_a Q96J87 ENSG00000140488 CELF6 96.90 9.20E-07 1.30E-10 65.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SYNCRIP HNRPQ NSAP1
Heterogeneous nuclear ribonucleoprotein Q (hnRNP Q) (Glycine- and tyrosine-rich RNA-binding protein) (GRY-RBP) (NS1-associated protein 1) (Synaptotagmin-binding, cytoplasmic RNA-interacting protein)
Homo sapiens
Amyotrophic Lateral Sclerosis 1,Spinal Muscular Atrophy,Myoblastoma,Autism Spectrum Disorder
2dgu_a O60506 ENSG00000135316 SYNCRIP 95.90 4.50E-05 6.00E-09 56.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBFOX1 A2BP A2BP1 FOX1 HRNBP1
RNA binding protein fox-1 homolog 1 (Ataxin-2-binding protein 1) (Fox-1 homolog A) (Hexaribonucleotide-binding protein 1)
Homo sapiens
Epilepsy,Atrial Heart Septal Defect,Myopia,Undetermined Early-Onset Epileptic Encephalopathy,Focal Epilepsy,Refractive Error,Developmental Coordination Disorder,Atrial Septal Defect 1,Conduct Disorder,Colorectal Cancer,Autosomal Dominant Cerebellar Ataxia,Benign Epilepsy With Centrotemporal Spikes,Disease Of Mental Health,Wheat Allergy,Dengue Shock Syndrome,Schizophrenia,Spinocerebellar Ataxia 2,Attention Deficit-Hyperactivity Disorder,Pervasive Developmental Disorder,Autism Spectrum Disorder,Atrial Septal Defect 2,Rett Syndrome,Autism,Epilepsy, Idiopathic Generalized
2n82_b Q9NWB1 ENSG00000078328 RBFOX1 96.20 1.60E-05 2.30E-09 55.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RNA15 YGL044C
mRNA 3'-end-processing protein RNA15
Saccharomyces cerevisiae
2km8_b P25299 96.50 6.10E-06 9.50E-10 53.90 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SMB1 YER029C
Small nuclear ribonucleoprotein-associated protein B (snRNP-B) (Sm protein B) (Sm-B) (SmB)
Saccharomyces cerevisiae
6g90_b P40018 96.60 5.70E-06 6.90E-10 75.40 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CIRBP A18HNRNP CIRP
Cold-inducible RNA-binding protein (A18 hnRNP) (Glycine-rich RNA-binding protein CIRP)
Homo sapiens
Acth-Secreting Pituitary Adenoma,Cryptorchidism, Unilateral Or Bilateral
1x5s_a Q14011 ENSG00000099622 CIRBP 96.30 1.10E-05 1.70E-09 54.50 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Dazl Dazl1 Dazla
Deleted in azoospermia-like (DAZ-like autosomal) (Deleted in azoospermia-like 1)
Mus musculus
2xs7_a Q64368 96.40 7.90E-06 1.10E-09 56.70 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ZCRB1
Zinc finger CCHC-type and RNA-binding motif-containing protein 1 (U11/U12 small nuclear ribonucleoprotein 31 kDa protein) (U11/U12 snRNP 31 kDa protein) (U11/U12-31K)
Homo sapiens
2e5h_a Q8TBF4 ENSG00000139168 ZCRB1 96.10 2.40E-05 3.70E-09 52.40 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
40S ribosomal protein S8
40S ribosomal protein S8
Oryctolagus cuniculus
5k0y_o G1TJW1 ENSG00000130811 EIF3G 96.30 1.10E-05 1.80E-09 51.20 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM4B RBM30
RNA-binding protein 4B (RNA-binding motif protein 30) (RNA-binding motif protein 4B) (RNA-binding protein 30)
Homo sapiens
Episodic Ataxia, Type 6
2dgt_a Q9BQ04 ENSG00000173914 RBM4B 95.70 6.40E-05 9.10E-09 52.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNRPB2
U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'')
Homo sapiens
Systemic Lupus Erythematosus
1a9n_d P08579 ENSG00000125870 SNRPB2 96.30 1.20E-05 1.60E-09 57.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
glo 110 46 anon-WO0118547.328 cg6946 Dmel\CG6946 Glo l(3)S011046 l(3)S11046 p67 p67-K CG6946 Dmel_CG6946
glo 110 46 anon-WO0118547.328 cg6946 Dmel\CG6946 Glo l(3)S011046 l(3)S11046 p67 p67-K CG6946 Dmel_CG6946
Drosophila melanogaster
5uzg_a Q9VGH5 95.70 5.60E-05 8.70E-09 50.90 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
HNRNPH1 HNRPH HNRPH1
Heterogeneous nuclear ribonucleoprotein H (hnRNP H) [Cleaved into: Heterogeneous nuclear ribonucleoprotein H, N-terminally processed]
Homo sapiens
Endometrial Stromal Sarcoma,Myopathy,Congenital Lymphedema,Myotonic Disease,Myotonic Dystrophy 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Spinocerebellar Ataxia 8,Atrial Septal Defect 1,Endometrial Stromal Tumor,Precursor T-Cell Acute Lymphoblastic Leukemia,Myotonic Dystrophy 2,Congenital Myasthenic Syndrome,Dermatopathia Pigmentosa Reticularis,Hereditary Lymphedema,Mental Retardation, X-Linked, Syndromic, Bain Type
2lxu_a P31943 ENSG00000169045 HNRNPH1 95.90 3.50E-05 5.40E-09 52.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Tia1 Tia
Nucleolysin TIA-1 (RNA-binding protein TIA-1) (T-cell-restricted intracellular antigen-1) (TIA-1)
Mus musculus
2rne_a P52912 97.00 8.00E-07 1.10E-10 65.10 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBMS2 SCR3
RNA-binding motif, single-stranded-interacting protein 2 (Suppressor of CDC2 with RNA-binding motif 3)
Homo sapiens
Variola Minor,Cone-Rod Dystrophy 2,Hemolytic Uremic Syndrome, Atypical 1
1x4e_a Q15434 ENSG00000076067 RBMS2 96.30 1.30E-05 1.90E-09 53.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Rbm28
RNA-binding protein 28 (RNA-binding motif protein 28)
Mus musculus
1x4h_a Q8CGC6 96.50 7.20E-06 9.50E-10 61.60 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
DAZAP1
DAZ-associated protein 1 (Deleted in azoospermia-associated protein 1)
Homo sapiens
Infertility,Azoospermia
2dgs_a Q96EP5 ENSG00000071626 DAZAP1 96.30 1.30E-05 2.00E-09 55.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
sup-12 CELE_T22B2.4 T22B2.4
sup-12 CELE_T22B2.4 T22B2.4
Caenorhabditis elegans
4ch0_s O45189 96.30 1.10E-05 1.60E-09 55.80 0 0 0 0 0 1 0 0
YBL051C PIN4 SGDID:S000000147
RBM12 KIAA0765 HRIHFB2091
RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN)
Homo sapiens
Psychotic Disorder,Schizoaffective Disorder,Schizophrenia 19,Schizophrenia
2ek1_g Q9NTZ6 ENSG00000244462 RBM12 97.00 8.40E-07 1.20E-10 63.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SFPQ PSF
Splicing factor, proline- and glutamine-rich (100 kDa DNA-pairing protein) (hPOMp100) (DNA-binding p52/p100 complex, 100 kDa subunit) (Polypyrimidine tract-binding protein-associated-splicing factor) (PSF) (PTB-associated-splicing factor)
Homo sapiens
Dyslexia,Childhood Kidney Cell Carcinoma,Parkinson Disease, Late-Onset,Pick Disease Of Brain,Perivascular Tumor,Renal Cell Carcinoma, Papillary, 1,Renal Cell Carcinoma, Xp11-Associated,Frontotemporal Dementia
6ncq_a P23246 ENSG00000116560 SFPQ 97.00 8.00E-07 1.00E-10 76.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
IGF2BP2 IMP2 VICKZ2
Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2 mRNA-binding protein 2) (IMP-2) (Hepatocellular carcinoma autoantigen p62) (IGF-II mRNA-binding protein 2) (VICKZ family member 2)
Homo sapiens
Diabetes Mellitus,Wolfram Syndrome 1,Testicular Cancer,Wolfram Syndrome,Hepatocellular Carcinoma,Type 2 Diabetes Mellitus,Maturity-Onset Diabetes Of The Young
2cqh_a Q9Y6M1 ENSG00000073792 IGF2BP2 96.30 1.10E-05 1.50E-09 57.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NAB3 HMD1 YPL190C
Nuclear polyadenylated RNA-binding protein 3
Saccharomyces cerevisiae
2kvi_a P38996 96.50 5.80E-06 7.70E-10 60.60 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122
RNA-binding protein 10 (G patch domain-containing protein 9) (RNA-binding motif protein 10) (RNA-binding protein S1-1) (S1-1)
Homo sapiens
Malignant Exocrine Pancreas Neoplasm,Atrial Heart Septal Defect,Skin Angiosarcoma,Colorectal Cancer,Microcephaly,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Renal Cell Carcinoma, Papillary, 1,Tarp Syndrome,Microcephalic Osteodysplastic Primordial Dwarfism, Type I
2lxi_a P98175 ENSG00000182872 RBM10 96.80 1.90E-06 2.80E-10 60.20 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3
Serine/arginine-rich splicing factor 1 (Alternative-splicing factor 1) (ASF-1) (Splicing factor, arginine/serine-rich 1) (pre-mRNA-splicing factor SF2, P33 subunit)
Homo sapiens
Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Myopathy,Homocystinuria,Rothmund-Thomson Syndrome, Type 2,Endometrial Stromal Tumor,Fanconi Anemia, Complementation Group A,Disease Of Mental Health,Retinitis Pigmentosa 4,Congenital Myasthenic Syndrome,Alzheimer Disease 3
1x4a_a Q07955 ENSG00000136450 SRSF1 96.20 1.80E-05 2.50E-09 57.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Tc00.1047053511727.270
Tc00.1047053511727.270
Trypanosoma cruzi
5opt_h Q4DY32 96.70 3.30E-06 4.20E-10 74.10 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
Rbm12
RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN)
Mus musculus
2cqp_a Q8R4X3 96.90 1.10E-06 1.50E-10 63.70 0 0 1 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
LDBPK_320790
LDBPK_320790
Leishmania donovani
5osg_h E9BNI3 96.60 5.20E-06 6.80E-10 70.70 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
HRP1 NAB4 NAB5 YOL123W
Nuclear polyadenylated RNA-binding protein 4 (Cleavage factor IB) (CFIB)
Saccharomyces cerevisiae
2cjk_a Q99383 96.50 5.50E-06 8.30E-10 62.10 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SSB
Lupus La protein (La autoantigen) (La ribonucleoprotein) (Sjoegren syndrome type B antigen) (SS-B)
Homo sapiens
Chronic Interstitial Cystitis,Chromosomal Disease,Mononeuritis Multiplex,Dyskinesia Of Esophagus,Connective Tissue Disease,Potocki-Shaffer Syndrome,Diffuse Infiltrative Lymphocytosis Syndrome,Mononeuropathy,Hemorrhagic Disease,Sjogren Syndrome,Polyclonal Hypergammaglobulinemia,Keratoconjunctivitis Sicca,Submandibular Gland Disease,Xerophthalmia,Heart Conduction Disease,Parotitis,Parotid Disease,Sialadenitis,Uveoparotid Fever,Orbital Granuloma,Undifferentiated Connective Tissue Disease,Lupus Erythematosus,Mononeuritis Of Upper Limb And Mononeuritis Multiplex,Lacrimal Apparatus Disease,Salivary Gland Disease,Endocardial Fibroelastosis,Hepatitis C Virus,Limited Scleroderma,Raynaud Disease,Heart Block, Congenital,Atrioventricular Block,Second-Degree Atrioventricular Block,Third-Degree Atrioventricular Block,Lymphoid Interstitial Pneumonia,Autoimmune Disease Of Exocrine System,Autoimmune Disease Of Musculoskeletal System,Munchausen By Proxy,Systemic Lupus Erythematosus,Chromosomal Deletion Syndrome
1s79_a P05455 ENSG00000138385 SSB 96.30 1.10E-05 1.70E-09 56.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PPIE CYP33
Peptidyl-prolyl cis-trans isomerase E (PPIase E) (EC 5.2.1.8) (Cyclophilin E) (Cyclophilin-33) (Rotamase E)
5.2.1.8 Homo sapiens
2cqb_a Q9UNP9 ENSG00000084072 PPIE 96.50 4.90E-06 7.20E-10 58.70 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBMS1 C2orf12 MSSP MSSP1 SCR2
RNA-binding motif, single-stranded-interacting protein 1 (Single-stranded DNA-binding protein MSSP-1) (Suppressor of CDC2 with RNA-binding motif 2)
Homo sapiens
Diffuse Glomerulonephritis,Epidermolysis Bullosa, Junctional, Herlitz Type,Hemolytic Uremic Syndrome, Atypical 1,Coffin-Siris Syndrome 1,Arthrogryposis Multiplex Congenita 2, Neurogenic Type
1x5o_a P29558 ENSG00000153250 RBMS1 96.80 1.70E-06 2.20E-10 66.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
HNRNPM HNRPM NAGR1
Heterogeneous nuclear ribonucleoprotein M (hnRNP M)
Homo sapiens
Spinal Muscular Atrophy,Bladder Clear Cell Adenocarcinoma,Contagious Pustular Dermatitis,Laryngotracheitis
2dh9_a P52272 ENSG00000099783 HNRNPM 96.00 2.70E-05 4.10E-09 51.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RNPS1 LDC2
RNA-binding protein with serine-rich domain 1 (SR-related protein LDC2)
Homo sapiens
Metaphyseal Chondrodysplasia, Schmid Type,Retinitis Pigmentosa
4a8x_a Q15287 ENSG00000205937 RNPS1 96.40 8.10E-06 1.30E-09 54.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PABPN1 PAB2 PABP2
Polyadenylate-binding protein 2 (PABP-2) (Poly(A)-binding protein 2) (Nuclear poly(A)-binding protein 1) (Poly(A)-binding protein II) (PABII) (Polyadenylate-binding nuclear protein 1)
Homo sapiens
Muscular Disease,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Autosomal Dominant Distal Myopathy,Muscular Dystrophy,Noonan Syndrome 1,Oculopharyngeal Muscular Dystrophy,Influenza,Dysphagia,Hand-Foot-Genital Syndrome,Partington X-Linked Mental Retardation Syndrome,Ptosis,Central Hypoventilation Syndrome, Congenital,Frontotemporal Dementia
3ucg_a Q86U42 ENSG00000100836 PABPN1 96.30 1.00E-05 1.50E-09 54.40 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ECC02_003561
ECC02_003561
Trypanosoma cruzi
1u6f_a Q967R0 96.10 2.70E-05 3.50E-09 61.30 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SETD1A KIAA0339 KMT2F SET1 SET1A
Histone-lysine N-methyltransferase SETD1A (EC 2.1.1.354) (Lysine N-methyltransferase 2F) (SET domain-containing protein 1A) (hSET1A) (Set1/Ash2 histone methyltransferase complex subunit SET1)
2.1.1.354 Homo sapiens
Neurodevelopmental Disorder With Speech Impairment And Dysmorphic Facies,Epilepsy,Nasal Cavity Benign Neoplasm,Myopathy, Centronuclear, 1,Malt Worker'S Lung,Prostate Squamous Cell Carcinoma,Primary Hyperoxaluria,Microcephaly,Kleefstra Syndrome 2,Disease Of Mental Health,Schizophrenia,Epilepsy, Early-Onset, With Or Without Developmental Delay,Kabuki Syndrome 1,Hyperinsulinemic Hypoglycemia, Familial, 1
3s8s_a O15047 ENSG00000099381 SETD1A 97.00 8.50E-07 1.20E-10 66.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM38 RNPC1 SEB4
RNA-binding protein 38 (CLL-associated antigen KW-5) (HSRNASEB) (RNA-binding motif protein 38) (RNA-binding region-containing protein 1) (ssDNA-binding protein SEB4)
Homo sapiens
Viral Exanthem,Erythema Infectiosum,Lung Cancer
2cqd_a Q9H0Z9 ENSG00000132819 RBM38 95.70 5.50E-05 8.50E-09 52.40 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PABPC1 PAB1 PABP1 PABPC2
Polyadenylate-binding protein 1 (PABP-1) (Poly(A)-binding protein 1)
Homo sapiens
Motor Neuron Disease,Rift Valley Fever,Waardenburg Syndrome, Type 4b,Myotonic Dystrophy 2,Waardenburg Syndrome, Type 4a,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Dengue Virus
2d9p_a P11940 ENSG00000070756 PABPC1 96.30 1.10E-05 1.60E-09 57.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM7
RNA-binding protein 7 (RNA-binding motif protein 7)
Homo sapiens
Pontocerebellar Hypoplasia
2m8h_a Q9Y580 ENSG00000076053 RBM7 96.20 1.50E-05 2.10E-09 56.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
MIP6 YHR015W
RNA-binding protein MIP6 (MEX67-interacting protein 6)
Saccharomyces cerevisiae
5d77_a P38760 95.80 4.50E-05 6.90E-09 49.70 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PSRP2 SOVF_116380
30S ribosomal protein 2, chloroplastic (Chloroplastic small ribosomal subunit protein cS22) (Plastid-specific 30S ribosomal protein 2) (PSRP-2)
Spinacia oleracea
5mmm_v P82277 97.00 9.30E-07 1.30E-10 75.30 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
EWSR1 EWS
RNA-binding protein EWS (EWS oncogene) (Ewing sarcoma breakpoint region 1 protein)
Homo sapiens
Retinitis Pigmentosa,Endometrial Stromal Sarcoma,Extraosseous Ewing Sarcoma,Clear Cell Sarcoma,Spindle Cell Sarcoma,Chondrosarcoma,Rhabdomyosarcoma 2,Sarcomatoid Basal Cell Carcinoma,Malignant Fibrous Histiocytoma,Melanoma,Rare Tumor,Cerebellar Angioblastoma,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Bladder Sarcoma,Melanoma Of Soft Tissue,Bone Epithelioid Hemangioma,Fibrous Histiocytoma,Peripheral Nervous System Neoplasm,Connective Tissue Cancer,Bone Sarcoma,Desmoplastic Small Round Cell Tumor,Constipation,Vulvar Sarcoma,Mucoepidermoid Carcinoma,Extraskeletal Mesenchymal Chondrosarcoma,Extraosseous Chondrosarcoma,Atypical Teratoid Rhabdoid Tumor,Astroblastoma,Intracranial Primitive Neuroectodermal Tumor,Neurofibromatosis, Type I,Sarcomatosis,Neuroblastoma,Myoepithelial Carcinoma,Cauda Equina Neoplasm,Childhood Malignant Schwannoma,Kidney Clear Cell Sarcoma,Middle Ear Carcinoma,Thymus Clear Cell Carcinoma,Extraosseous Ewings Sarcoma-Primitive Neuroepithelial Tumor,Essential Tremor,Central Nervous System Mesenchymal Non-Meningothelial Tumor,Congenital Fibrosarcoma,Autonomic Nervous System Neoplasm,Myoepithelioma,Endometrial Stromal Tumor,Sweat Gland Benign Neoplasm,Synovium Cancer,Small Intestinal Sarcoma,Bladder Leiomyoma,Extraskeletal Ewing Sarcoma,Lung Sarcoma,Endobronchial Lipoma,Cranial Nerve Malignant Neoplasm,Ring Chromosome,Biphasic Synovial Sarcoma,Epithelioid Cell Synovial Sarcoma,Well-Differentiated Liposarcoma,Cellular Myxoid Liposarcoma,Pleomorphic Liposarcoma,Peripheral Nervous System Disease,Small Cell Sarcoma,Sweat Gland Disease,Myxoid Chondrosarcoma,Skin Benign Neoplasm,Kidney Fibrosarcoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Myxoid Liposarcoma,Myasthenic Syndrome, Congenital, 5,Sarcoma,Mesenchymal Cell Neoplasm,Fibrosarcoma,Localized Osteosarcoma,Ewing Sarcoma Of Bone,Bone Osteosarcoma,Small Cell Osteogenic Sarcoma,Conventional Central Osteosarcoma,Cranial Nerve Neoplasm,Liposarcoma,Pediatric Fibrosarcoma,Congenital Myasthenic Syndrome,Olfactory Nerve Neoplasm,Rhabdoid Cancer,Kidney Rhabdoid Cancer,Olfactory Neuroblastoma,Extracranial Neuroblastoma,Extraskeletal Chondroma,Skeletal Muscle Cancer,Muscle Cancer,Sarcoma, Synovial,Askin'S Tumor,Ewing Sarcoma,Chondrosarcoma, Extraskeletal Myxoid,Cervical Neuroblastoma,Wilms Tumor 1,Connective Tissue Benign Neoplasm,Lipomatosis, Multiple
2cpe_a Q01844 ENSG00000182944 EWSR1 96.80 1.60E-06 2.10E-10 66.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
MTHFSD
Methenyltetrahydrofolate synthase domain-containing protein
Homo sapiens
Amyotrophic Lateral Sclerosis 1,Feingold Syndrome 1,Intestinal Atresia,Pancreas, Annular,Vacterl Association,Gastrointestinal Defects And Immunodeficiency Syndrome,Pallister-Hall Syndrome,Microphthalmia, Syndromic 3,Anus, Imperforate
2e5j_a Q2M296 ENSG00000103248 MTHFSD 96.70 3.00E-06 4.20E-10 60.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
NUP35 MP44 NUP53
Nucleoporin NUP35 (35 kDa nucleoporin) (Mitotic phosphoprotein 44) (MP-44) (Nuclear pore complex protein Nup53) (Nucleoporin NUP53)
Homo sapiens
Achalasia-Addisonianism-Alacrima Syndrome,Seminal Vesicle Tumor,Male Reproductive Organ Benign Neoplasm,Lethal Congenital Contracture Syndrome 1
4lir_b Q8NFH5 ENSG00000163002 NUP35 96.30 1.50E-05 1.60E-09 65.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PF3D7_1320900
PF3D7_1320900
Plasmodium falciparum
2myf_a C0H5C7 96.60 3.60E-06 5.70E-10 55.40 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SPEN KIAA0929 MINT SHARP
Msx2-interacting protein (SMART/HDAC1-associated repressor protein) (SPEN homolog)
Homo sapiens
Gastrointestinal Neuroendocrine Benign Tumor,Spleen Cancer,Gastric Neuroendocrine Neoplasm,Breast Liposarcoma,Wolfram Syndrome 2,Mullegama-Klein-Martinez Syndrome,Chromosome 1p36 Deletion Syndrome
4p6q_a Q96T58 ENSG00000065526 SPEN 96.40 1.10E-05 1.30E-09 72.60 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SYF2 CBPIN GCIPIP
Pre-mRNA-splicing factor SYF2 (CCNDBP1-interactor) (p29)
Homo sapiens
6qdv_y O95926 ENSG00000117614 SYF2 96.40 7.70E-06 1.10E-09 57.50 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
PTBP2 NPTB PTB PTBLP
Polypyrimidine tract-binding protein 2 (Neural polypyrimidine tract-binding protein) (Neurally-enriched homolog of PTB) (PTB-like protein)
Homo sapiens
Cancer-Associated Retinopathy,Patellar Tendinitis
4cq1_b Q9UKA9 ENSG00000117569 PTBP2 96.60 3.40E-06 5.00E-10 66.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
ELAVL4 HUD PNEM
ELAV-like protein 4 (Hu-antigen D) (HuD) (Paraneoplastic encephalomyelitis antigen HuD)
Homo sapiens
Retinitis Pigmentosa,Myotonic Dystrophy 1,Paraneoplastic Neurologic Disorders,Pontocerebellar Hypoplasia, Type 7,Spinal Muscular Atrophy,Motor Neuron Disease,Muscular Atrophy,Neuroblastoma,Sensory Peripheral Neuropathy,Hallucinogen Abuse,Atrial Septal Defect 1,Cone-Rod Dystrophy 6,Parkinson Disease, Late-Onset,Hyperinsulinemic Hypoglycemia, Familial, 4,Disease Of Mental Health,Retinitis Pigmentosa 49,Scalp-Ear-Nipple Syndrome,Fragile X Syndrome,Lambert-Eaton Myasthenic Syndrome,Lung Cancer
1fxl_a P26378 ENSG00000162374 ELAVL4 96.80 1.50E-06 2.20E-10 65.70 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
snf D25 fs(1)1621 liz CG4528
U1 small nuclear ribonucleoprotein A (U1 snRNP A) (U1-A) (U1A) (Sex determination protein snf)
Drosophila melanogaster
2b0g_a P43332 96.50 5.80E-06 8.10E-10 57.40 0 0 0 0 1 0 0 0
YBL051C PIN4 SGDID:S000000147
SART3 KIAA0156 TIP110
Squamous cell carcinoma antigen recognized by T-cells 3 (SART-3) (Tat-interacting protein of 110 kDa) (Tip110) (p110 nuclear RNA-binding protein)
Homo sapiens
Porokeratosis
2do4_a Q15020 ENSG00000075856 SART3 96.60 4.30E-06 6.20E-10 59.50 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
msl1 pi056 SPBC8D2.09c
Probable U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'')
Schizosaccharomyces pombe
3jb9_k Q7LL14 96.60 3.60E-06 4.80E-10 62.80 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CELF1 BRUNOL2 CUGBP CUGBP1 NAB50
CUGBP Elav-like family member 1 (CELF-1) (50 kDa nuclear polyadenylated RNA-binding protein) (Bruno-like protein 2) (CUG triplet repeat RNA-binding protein 1) (CUG-BP1) (CUG-BP- and ETR-3-like factor 1) (Deadenylation factor CUG-BP) (Embryo deadenylation element-binding protein homolog) (EDEN-BP homolog) (RNA-binding protein BRUNOL-2)
Homo sapiens
Neuromuscular Disease,Myotonic Disease,Myotonic Dystrophy 1,Neurofibromatosis, Type I,Muscular Dystrophy,Myotonic Dystrophy,Spinocerebellar Ataxia 8,Oculopharyngeal Muscular Dystrophy,Myotonic Dystrophy 2,Lens Disease,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Fragile X Syndrome,Huntington Disease-Like 2,Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Spinal And Bulbar Muscular Atrophy, X-Linked 1
2rqc_a Q92879 ENSG00000149187 CELF1 96.80 1.50E-06 2.10E-10 64.10 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
asd-1 CELE_R74.5 R74.5
asd-1 CELE_R74.5 R74.5
Caenorhabditis elegans
2mgz_a G5EEW7 96.00 2.80E-05 4.10E-09 53.00 0 0 0 0 0 1 0 0
YBL051C PIN4 SGDID:S000000147
RBM42
RNA-binding protein 42 (RNA-binding motif protein 42)
Homo sapiens
6qw6_r Q9BTD8 ENSG00000126254 RBM42 97.20 3.60E-07 3.70E-11 93.10 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SNRPC
U1 small nuclear ribonucleoprotein C (U1 snRNP C) (U1-C) (U1C)
Homo sapiens
Autoimmune Disease,Atrial Septal Defect 2
6eld_a P09234 ENSG00000124562 SNRPC 96.50 7.00E-06 9.30E-10 64.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SF3B6 SAP14 SF3B14 SF3B14A CGI-110 HSPC175 HT006
Splicing factor 3B subunit 6 (Pre-mRNA branch site protein p14) (SF3b 14 kDa subunit) (SF3B14a) (Spliceosome-associated protein, 14-kDa) (Splicing factor 3b, subunit 6, 14kDa)
Homo sapiens
Amyotrophic Lateral Sclerosis 1
2fho_b Q9Y3B4 ENSG00000115128 SF3B6 95.80 4.50E-05 6.50E-09 51.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
FUS TLS
RNA-binding protein FUS (75 kDa DNA-pairing protein) (Oncogene FUS) (Oncogene TLS) (POMp75) (Translocated in liposarcoma protein)
Homo sapiens
Amyotrophic Lateral Sclerosis 6 With Or Without Frontotemporal Dementia,Lattice Corneal Dystrophy,Tremor, Hereditary Essential, 4,Amyotrophic Lateral Sclerosis 18,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Anal Carcinoma In Situ,Amyotrophic Lateral Sclerosis 11,Clear Cell Sarcoma,Tremor,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Neuromuscular Disease,Fibrous Histiocytoma,Connective Tissue Cancer,Progressive Bulbar Palsy,Pica Disease,Dysgraphia,Nominal Aphasia,Extraosseous Chondrosarcoma,Amyotrophic Lateral Sclerosis 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Ideomotor Apraxia,Giant Axonal Neuropathy 2,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Spinal Muscular Atrophy,Motor Neuron Disease,Movement Disease,Muscular Atrophy,Locked-In Syndrome,Essential Tremor,Multisystem Proteinopathy,Synovium Cancer,Dementia,Cerebellar Disease,Juvenile Amyotrophic Lateral Sclerosis,Chondroid Lipoma,Dystonia,Myeloid Leukemia,Tremor, Hereditary Essential, 2,Well-Differentiated Liposarcoma,Cellular Myxoid Liposarcoma,Pediatric Liposarcoma,Pleomorphic Liposarcoma,Mixed Liposarcoma,Sclerosing Liposarcoma,Amyotrophic Lateral Sclerosis 4, Juvenile,Speech And Communication Disorders,Progressive Muscular Atrophy,Kidney Fibrosarcoma,Rhabdomyosarcoma,Pick Disease Of Brain,Myxoid Liposarcoma,Autosomal Dominant Cerebellar Ataxia,Sarcoma,Fibrosarcoma,Liposarcoma,Disease Of Mental Health,Dentatorubral-Pallidoluysian Atrophy,Dermatopathia Pigmentosa Reticularis,Dementia, Lewy Body,Hemochromatosis, Type 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4,Sarcoma, Synovial,Spinocerebellar Ataxia 2,Tremor, Hereditary Essential, 3,Amyotrophic Lateral Sclerosis 21,Amyotrophic Lateral Sclerosis 9,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia,Tremor, Hereditary Essential, 1,Ewing Sarcoma,Amyotrophic Lateral Sclerosis 16, Juvenile,Chondrosarcoma, Extraskeletal Myxoid,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3,Epilepsy, Familial Temporal Lobe, 8,Fragile X-Associated Tremor/Ataxia Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Autism Spectrum Disorder,Aphasia,Writing Disorder,Associative Agnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 12,Amyotrophic Lateral Sclerosis Type 14,Lipomatosis, Multiple,Amyotrophic Lateral Sclerosis Type 22,Epithelial-Stromal Tgfbi Dystrophy,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7
2la6_a P35637 ENSG00000089280 FUS 96.60 4.30E-06 5.20E-10 63.90 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
RBM11
Splicing regulator RBM11 (RNA-binding motif protein 11)
Homo sapiens
2ywk_a P57052 ENSG00000185272 RBM11 96.30 1.20E-05 1.80E-09 55.30 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
TIAL1
Nucleolysin TIAR (TIA-1-related protein)
Homo sapiens
Ulcerative Blepharitis,Spinal Muscular Atrophy,Salpingitis Isthmica Nodosa
1x4g_a Q01085 ENSG00000151923 TIAL1 96.40 8.60E-06 1.20E-09 60.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CPSF6 CFIM68
Cleavage and polyadenylation specificity factor subunit 6 (Cleavage and polyadenylation specificity factor 68 kDa subunit) (CPSF 68 kDa subunit) (Cleavage factor Im complex 68 kDa subunit) (CFIm68) (Pre-mRNA cleavage factor Im 68 kDa subunit) (Protein HPBRII-4/7)
Homo sapiens
Acute Promyelocytic Leukemia,Carnitine-Acylcarnitine Translocase Deficiency
3p5t_o Q16630 ENSG00000111605 CPSF6 96.60 3.70E-06 5.30E-10 58.80 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
CPSF7
Cleavage and polyadenylation specificity factor subunit 7 (Cleavage and polyadenylation specificity factor 59 kDa subunit) (CPSF 59 kDa subunit) (Cleavage factor Im complex 59 kDa subunit) (CFIm59) (Pre-mRNA cleavage factor Im 59 kDa subunit)
Homo sapiens
3n9u_i Q8N684 ENSG00000149532 CPSF7 96.00 3.20E-05 4.30E-09 60.70 0 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
SDN1 At3g50100 F3A4.180
Small RNA degrading nuclease 1 (EC 3.1.-.-)
3.1.-.- Arabidopsis thaliana
5z9z_a A3KPE8 96.60 6.60E-06 6.40E-10 68.70 0 0 0 0 0 0 1 0
YBL051C PIN4 SGDID:S000000147
RNPC3 KIAA1839 RBM40 RNP SNRNP65
RNA-binding region-containing protein 3 (RNA-binding motif protein 40) (RNA-binding protein 40) (U11/U12 small nuclear ribonucleoprotein 65 kDa protein) (U11/U12 snRNP 65 kDa protein) (U11/U12-65K)
Homo sapiens
Connective Tissue Disease,Parainfluenza Virus Type 3,Sjogren Syndrome,Growth Hormone Deficiency,Mixed Connective Tissue Disease,Limited Scleroderma,Isolated Growth Hormone Deficiency, Type V,Systemic Lupus Erythematosus,Isolated Growth Hormone Deficiency,Microcephalic Osteodysplastic Primordial Dwarfism, Type I,Isolated Growth Hormone Deficiency, Type Ia
5obn_a Q96LT9 ENSG00000185946 RNPC3 97.00 7.10E-07 8.40E-11 73.00 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
EIF3G EIF3S4
Eukaryotic translation initiation factor 3 subunit G (eIF3g) (Eukaryotic translation initiation factor 3 RNA-binding subunit) (eIF-3 RNA-binding subunit) (Eukaryotic translation initiation factor 3 subunit 4) (eIF-3-delta) (eIF3 p42) (eIF3 p44)
Homo sapiens
Narcolepsy
2cq0_a O75821 ENSG00000130811 EIF3G 96.50 5.40E-06 7.90E-10 58.30 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
TRNAU1AP SECP43 TRSPAP1
tRNA selenocysteine 1-associated protein 1 (SECp43) (tRNA selenocysteine-associated protein 1)
Homo sapiens
Combined D-2- And L-2-Hydroxyglutaric Aciduria,Ivic Syndrome,Ischiocoxopodopatellar Syndrome With Or Without Pulmonary Arterial Hypertension
2div_a Q9NX07 ENSG00000180098 TRNAU1AP 96.50 5.90E-06 8.40E-10 58.40 1 1 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
GBP2 RLF6 YCL011C YCL11C
Single-strand telomeric DNA-binding protein GBP2 (G-strand-binding protein 2) (RAP1 localization factor 6)
Saccharomyces cerevisiae
2mzq_a P25555 96.80 1.60E-06 2.20E-10 62.30 0 0 0 0 0 0 0 0
YBL051C PIN4 SGDID:S000000147
IST3 SNU17 YIR005W YIB5W
U2 snRNP component IST3 (Increased sodium tolerance protein 3) (U2 snRNP protein SNU17)
Saccharomyces cerevisiae
2my2_a P40565 96.70 2.60E-06 3.40E-10 64.30 0 0 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab