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

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YNL197C WHI3 / SGDID:S000005141
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
YNL197C WHI3 SGDID:S000005141
Sxl Sx1 CG43770
Protein sex-lethal
Drosophila melanogaster
1b7f_b P19339 95.40 0.00012 1.80E-08 54.00 0 0 0 0 1 0 0 0
YNL197C WHI3 SGDID:S000005141
SYF2 NTC31 YGR129W
Pre-mRNA-splicing factor SYF2 (PRP19 complex protein 31) (Synthetic lethal with CDC40 protein 2)
Saccharomyces cerevisiae
6exn_y P53277 95.50 0.0001 1.40E-08 55.20 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
Rbm12
RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN)
Mus musculus
2cqp_a Q8R4X3 95.40 0.00013 1.90E-08 51.70 0 0 1 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
mec-8 CELE_F46A9.6 F46A9.6
mec-8 CELE_F46A9.6 F46A9.6
Caenorhabditis elegans
5tkz_b G5ECJ4 95.30 0.00016 2.30E-08 50.60 0 0 0 0 0 1 0 0
YNL197C WHI3 SGDID:S000005141
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 95.20 0.00022 2.70E-08 53.60 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
2mhn_a Q14498 ENSG00000131051 RBM39 95.20 0.0002 2.90E-08 48.60 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
HSH49 YOR319W O6142
Protein HSH49
Saccharomyces cerevisiae
5lsb_c Q99181 95.60 7.40E-05 1.10E-08 58.70 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
3lqv_a Q9Y3B4 ENSG00000115128 SF3B6 95.20 0.00021 2.90E-08 52.40 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
1ha1_a P09651 ENSG00000135486 HNRNPA1 95.10 0.0002 3.00E-08 53.80 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
PRP24 YMR268C YM8156.10C
U4/U6 snRNA-associated-splicing factor PRP24 (U4/U6 snRNP protein)
Saccharomyces cerevisiae
2kh9_a P49960 95.10 0.00021 3.00E-08 49.80 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.00 0.00029 4.00E-08 49.40 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
Hnrnpl Fblim1
Heterogeneous nuclear ribonucleoprotein L (hnRNP L)
Rattus norvegicus
2mqn_a F1LQ48 96.10 2.00E-05 3.00E-09 62.20 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 96.00 3.70E-05 4.70E-09 58.70 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.40 0.00013 1.80E-08 54.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.10 0.00021 2.90E-08 51.40 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.70 6.10E-05 9.10E-09 57.80 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
4pkd_b P08621 ENSG00000104852 SNRNP70 96.40 8.00E-06 1.20E-09 67.70 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
MSL1 YIR009W YIB9W
U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'')
Saccharomyces cerevisiae
6j6g_a P40567 95.50 0.00012 1.50E-08 55.10 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.40 0.00012 1.70E-08 51.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.50 0.0001 1.60E-08 54.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.20 0.00022 2.70E-08 63.80 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.50 0.00011 1.60E-08 52.20 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.80 5.30E-05 7.60E-09 52.90 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.60 9.20E-05 1.20E-08 69.90 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
PES4 YFR023W
Protein PES4 (DNA polymerase epsilon suppressor 4)
Saccharomyces cerevisiae
6exx_a P39684 95.40 0.00012 1.90E-08 47.90 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.10 0.0002 2.90E-08 49.00 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.90 4.00E-05 5.70E-09 54.20 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
2rrb_a P62995 ENSG00000136527 TRA2B 95.00 0.00024 3.80E-08 46.60 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
gw GW182 CG31992
Protein Gawky
Drosophila melanogaster
2wbr_a Q8SY33 95.50 0.0001 1.40E-08 51.70 0 0 0 0 1 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.20 0.0002 2.80E-08 52.30 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
HRB1 TOM34 YNL004W N2009
Protein HRB1 (Protein TOM34)
Saccharomyces cerevisiae
2mzr_a P38922 95.10 0.00021 3.10E-08 49.20 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.00 0.00025 3.60E-08 49.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
LARP6
La-related protein 6 (Acheron) (Achn) (La ribonucleoprotein domain family member 6)
Homo sapiens
Brittle Bone Disorder
2mtg_a Q9BRS8 ENSG00000166173 LARP6 95.50 0.00014 1.50E-08 59.80 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.60 9.50E-05 1.20E-08 54.10 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
4f02_a P11940 ENSG00000070756 PABPC1 95.20 0.0002 2.90E-08 56.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
HNRNPM HNRPM NAGR1
Heterogeneous nuclear ribonucleoprotein M (hnRNP M)
Homo sapiens
Spinal Muscular Atrophy,Bladder Clear Cell Adenocarcinoma,Contagious Pustular Dermatitis,Laryngotracheitis
2do0_a P52272 ENSG00000099783 HNRNPM 95.00 0.00028 3.90E-08 51.00 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.60 8.70E-05 1.20E-08 54.80 0 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
SNRPA
SNRPA
Oryctolagus cuniculus
6cmn_a G1TM83 95.60 0.00011 1.30E-08 57.90 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
6dhs_d P31943 ENSG00000169045 HNRNPH1 95.00 0.00024 3.60E-08 54.10 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
LSM6 YDR378C D9481.18
U6 snRNA-associated Sm-like protein LSm6
Saccharomyces cerevisiae
5zwm_x Q06406 95.20 0.00022 2.80E-08 56.10 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.50 0.00011 1.30E-08 59.10 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 96.20 1.50E-05 2.20E-09 61.80 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.20 0.00019 2.60E-08 55.30 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.30 0.00016 2.20E-08 49.40 0 0 0 0 1 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.50 0.00011 1.40E-08 61.00 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
SDN1 At3g50100 F3A4.180
Small RNA degrading nuclease 1 (EC 3.1.-.-)
3.1.-.- Arabidopsis thaliana
5z9z_a A3KPE8 96.30 2.00E-05 1.90E-09 65.40 0 0 0 0 0 0 1 0
YNL197C WHI3 SGDID:S000005141
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 95.90 3.70E-05 5.50E-09 59.20 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
TIAL1
Nucleolysin TIAR (TIA-1-related protein)
Homo sapiens
Ulcerative Blepharitis,Spinal Muscular Atrophy,Salpingitis Isthmica Nodosa
1x4g_a Q01085 ENSG00000151923 TIAL1 95.00 0.00026 3.60E-08 51.20 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
RBM41
RNA-binding protein 41 (RNA-binding motif protein 41)
Homo sapiens
2cpx_a Q96IZ5 ENSG00000089682 RBM41 95.20 0.00017 2.40E-08 52.50 0 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.40 0.00012 1.70E-08 51.00 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
NCL
Nucleolin (Protein C23)
Mesocricetus auratus
1fj7_a P08199 95.70 6.40E-05 8.70E-09 54.40 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
SMB1 YER029C
Small nuclear ribonucleoprotein-associated protein B (snRNP-B) (Sm protein B) (Sm-B) (SmB)
Saccharomyces cerevisiae
6g90_b P40018 95.00 0.0003 3.70E-08 63.20 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
CPEB4 KIAA1673
Cytoplasmic polyadenylation element-binding protein 4 (CPE-BP4) (CPE-binding protein 4) (hCPEB-4)
Homo sapiens
2mki_a Q17RY0 ENSG00000113742 CPEB4 95.10 0.00021 3.00E-08 55.50 0 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
2g4b_a P26368 ENSG00000063244 U2AF2 95.10 0.00022 3.40E-08 52.50 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.70 6.30E-05 8.70E-09 63.00 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
3nmr_a Q92879 ENSG00000149187 CELF1 95.30 0.00016 2.40E-08 53.70 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.00 0.00026 4.00E-08 47.60 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
NAB3 HMD1 YPL190C
Nuclear polyadenylated RNA-binding protein 3
Saccharomyces cerevisiae
2kvi_a P38996 95.00 0.00026 3.50E-08 50.90 0 0 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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
6ah0_4 Q15427 ENSG00000143368 SF3B4 95.80 5.80E-05 6.70E-09 72.80 1 1 0 0 0 0 0 0
YNL197C WHI3 SGDID:S000005141
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 95.50 0.0001 1.50E-08 57.30 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab