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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 |
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YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.20 | 0.00021 | 2.80E-08 | 51.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.00 | 0.0003 | 3.90E-08 | 53.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.00 | 3.20E-05 | 4.20E-09 | 56.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | NCL |
Nucleolin (Protein C23) |
Mesocricetus auratus | 1fj7_a | P08199 | 95.80 | 6.50E-05 | 8.20E-09 | 57.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.90 | 4.00E-05 | 5.20E-09 | 57.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | EIF3B EIF3S9 |
Eukaryotic translation initiation factor 3 subunit B (eIF3b) (Eukaryotic translation initiation factor 3 subunit 9) (Prt1 homolog) (hPrt1) (eIF-3-eta) (eIF3 p110) (eIF3 p116) |
Homo sapiens | Noonan Syndrome 7,Mouth Disease |
5k1h_b | P55884 | ENSG00000106263 | EIF3B | 95.00 | 0.00028 | 4.00E-08 | 64.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.50 | 0.00012 | 1.50E-08 | 57.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 7.20E-05 | 9.20E-09 | 55.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.10 | 3.00E-05 | 3.50E-09 | 72.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 5uzn_a | Q9VGH5 | 95.30 | 0.00018 | 2.30E-08 | 52.30 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | Hnrnpl Fblim1 |
Heterogeneous nuclear ribonucleoprotein L (hnRNP L) |
Rattus norvegicus | 2mqn_a | F1LQ48 | 96.00 | 3.50E-05 | 4.70E-09 | 64.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | Sxl Sx1 CG43770 |
Protein sex-lethal |
Drosophila melanogaster | 2sxl_a | P19339 | 95.80 | 5.80E-05 | 8.20E-09 | 52.20 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | MSL1 YIR009W YIB9W |
U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'') |
Saccharomyces cerevisiae | 6j6g_a | P40567 | 95.80 | 5.50E-05 | 6.60E-09 | 59.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 6.70E-05 | 9.30E-09 | 53.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | gw GW182 CG31992 |
Protein Gawky |
Drosophila melanogaster | 2wbr_a | Q8SY33 | 95.80 | 6.30E-05 | 8.00E-09 | 55.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | UPF3B RENT3B UPF3X |
Regulator of nonsense transcripts 3B (Nonsense mRNA reducing factor 3B) (Up-frameshift suppressor 3 homolog B) (hUpf3B) (Up-frameshift suppressor 3 homolog on chromosome X) (hUpf3p-X) |
Homo sapiens | Metaphyseal Chondrodysplasia, Schmid Type,X-Linked Intellectual Disability With Marfanoid Habitus,Pancreatic Adenosquamous Carcinoma,Microcephaly,Disease Of Mental Health,Fryns Syndrome,Spermatogenic Failure 24,Non-Syndromic X-Linked Intellectual Disability,Opitz-Kaveggia Syndrome,Autism |
1uw4_a | Q9BZI7 | ENSG00000125351 | UPF3B | 95.10 | 0.00031 | 3.30E-08 | 56.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | SYF2 CBPIN GCIPIP |
Pre-mRNA-splicing factor SYF2 (CCNDBP1-interactor) (p29) |
Homo sapiens | 6qdv_y | O95926 | ENSG00000117614 | SYF2 | 95.00 | 0.00027 | 3.50E-08 | 51.30 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 3.50E-05 | 4.10E-09 | 61.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | Tia1 Tia |
Nucleolysin TIA-1 (RNA-binding protein TIA-1) (T-cell-restricted intracellular antigen-1) (TIA-1) |
Mus musculus | 2rne_a | P52912 | 95.50 | 0.00011 | 1.40E-08 | 55.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | Dazl Dazl1 Dazla |
Deleted in azoospermia-like (DAZ-like autosomal) (Deleted in azoospermia-like 1) |
Mus musculus | 2xs7_a | Q64368 | 96.10 | 2.10E-05 | 2.80E-09 | 56.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.30 | 0.00018 | 2.30E-08 | 54.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.10 | 0.00026 | 3.50E-08 | 51.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | SDN1 At3g50100 F3A4.180 |
Small RNA degrading nuclease 1 (EC 3.1.-.-) |
3.1.-.- | Arabidopsis thaliana | 5z9z_a | A3KPE8 | 97.30 | 2.60E-07 | 2.40E-11 | 79.40 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDL167C | NRP1 | SGDID:S000002326 | 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 |
5mpg_a | P09651 | ENSG00000135486 | HNRNPA1 | 95.30 | 0.00015 | 2.00E-08 | 52.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | PES4 YFR023W |
Protein PES4 (DNA polymerase epsilon suppressor 4) |
Saccharomyces cerevisiae | 6exx_a | P39684 | 95.60 | 7.80E-05 | 1.10E-08 | 51.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.50 | 0.00013 | 1.50E-08 | 68.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 6.70E-05 | 8.90E-09 | 55.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.20 | 2.50E-05 | 2.60E-09 | 66.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | RBM42 |
RNA-binding protein 42 (RNA-binding motif protein 42) |
Homo sapiens | 6qw6_r | Q9BTD8 | ENSG00000126254 | RBM42 | 95.20 | 0.00029 | 2.80E-08 | 73.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 6.90E-05 | 8.80E-09 | 55.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.20 | 0.00021 | 2.80E-08 | 51.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.00 | 3.50E-05 | 4.90E-09 | 60.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 5.30E-05 | 7.00E-09 | 55.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.80 | 2.00E-06 | 2.20E-10 | 75.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDL167C | NRP1 | SGDID:S000002326 | DAZAP1 |
DAZ-associated protein 1 (Deleted in azoospermia-associated protein 1) |
Homo sapiens | Infertility,Azoospermia |
2dgs_a | Q96EP5 | ENSG00000071626 | DAZAP1 | 95.30 | 0.00017 | 2.40E-08 | 51.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.90 | 4.20E-05 | 5.70E-09 | 62.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 |
2nz4_b | P09012 | ENSG00000077312 | SNRPA | 95.60 | 9.50E-05 | 1.20E-08 | 54.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | HRB1 TOM34 YNL004W N2009 |
Protein HRB1 (Protein TOM34) |
Saccharomyces cerevisiae | 2mzs_a | P38922 | 95.50 | 0.00011 | 1.40E-08 | 54.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 6.50E-05 | 8.60E-09 | 54.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.00 | 0.00029 | 4.00E-08 | 48.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | PF3D7_0517300 |
PF3D7_0517300 |
Plasmodium falciparum | 2n7c_a | Q8I3T5 | 95.20 | 0.00021 | 2.80E-08 | 50.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.10 | 0.00025 | 3.30E-08 | 51.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.60 | 5.20E-06 | 6.30E-10 | 64.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.50 | 0.0001 | 1.40E-08 | 59.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 5.40E-05 | 7.10E-09 | 56.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | PRP24 YMR268C YM8156.10C |
U4/U6 snRNA-associated-splicing factor PRP24 (U4/U6 snRNP protein) |
Saccharomyces cerevisiae | 2kh9_a | P49960 | 95.50 | 0.00011 | 1.40E-08 | 54.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | CPEB4 KIAA1673 |
Cytoplasmic polyadenylation element-binding protein 4 (CPE-BP4) (CPE-binding protein 4) (hCPEB-4) |
Homo sapiens | 2mki_a | Q17RY0 | ENSG00000113742 | CPEB4 | 95.70 | 7.20E-05 | 9.80E-09 | 61.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 5.80E-05 | 7.40E-09 | 56.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.30 | 0.00017 | 2.20E-08 | 52.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | SNRPB2 |
U2 small nuclear ribonucleoprotein B'' (U2 snRNP B'') |
Homo sapiens | Systemic Lupus Erythematosus |
1a9n_d | P08579 | ENSG00000125870 | SNRPB2 | 95.10 | 0.00022 | 2.90E-08 | 52.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | MUD1 YBR119W YBR0915 |
U1 small nuclear ribonucleoprotein A (U1 snRNP A) (U1-A) (U1A) (Mutant U1 die protein 1) |
Saccharomyces cerevisiae | 5zwn_s | P32605 | 95.50 | 0.00012 | 1.40E-08 | 66.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.60 | 8.60E-05 | 1.20E-08 | 51.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | LSM6 YDR378C D9481.18 |
U6 snRNA-associated Sm-like protein LSm6 |
Saccharomyces cerevisiae | 5zwm_x | Q06406 | 95.30 | 0.00019 | 2.30E-08 | 59.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 6.40E-05 | 8.10E-09 | 58.20 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | HSH49 YOR319W O6142 |
Protein HSH49 |
Saccharomyces cerevisiae | 5lsb_c | Q99181 | 96.00 | 3.60E-05 | 4.90E-09 | 63.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | Eif4h Wbscr1 |
Eukaryotic translation initiation factor 4H (eIF-4H) (Williams-Beuren syndrome chromosomal region 1 protein homolog) |
Mus musculus | 2dng_a | Q9WUK2 | 95.20 | 0.0002 | 2.60E-08 | 53.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | SNRPA |
SNRPA |
Oryctolagus cuniculus | 6cmn_a | G1TM83 | 96.10 | 2.80E-05 | 3.20E-09 | 64.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.20 | 0.00022 | 2.70E-08 | 63.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 0.00017 | 2.20E-08 | 51.70 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 |
6gd1_a | Q15717 | ENSG00000066044 | ELAVL1 | 96.00 | 3.80E-05 | 4.90E-09 | 64.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.40 | 0.00014 | 1.70E-08 | 54.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | Rcan1 Dscr1 |
Calcipressin-1 (Down syndrome critical region protein 1 homolog) (Myocyte-enriched calcineurin-interacting protein 1) (MCIP1) (Regulator of calcineurin 1) |
Mus musculus | 1wey_a | Q9JHG6 | 95.20 | 0.00024 | 2.70E-08 | 56.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.00 | 3.70E-05 | 4.60E-09 | 76.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.10 | 2.20E-05 | 3.00E-09 | 63.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | SYF2 NTC31 YGR129W |
Pre-mRNA-splicing factor SYF2 (PRP19 complex protein 31) (Synthetic lethal with CDC40 protein 2) |
Saccharomyces cerevisiae | 6exn_y | P53277 | 96.00 | 4.00E-05 | 4.90E-09 | 60.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.40 | 0.00014 | 1.70E-08 | 57.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.20 | 2.10E-05 | 2.30E-09 | 66.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.10 | 0.00025 | 3.40E-08 | 51.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | nono-1 CELE_F25B5.7 F25B5.7 |
nono-1 CELE_F25B5.7 F25B5.7 |
Caenorhabditis elegans | 5ca5_a | B3GWA1 | 95.80 | 6.40E-05 | 7.90E-09 | 67.10 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.30 | 0.00016 | 2.20E-08 | 53.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | SMB1 YER029C |
Small nuclear ribonucleoprotein-associated protein B (snRNP-B) (Sm protein B) (Sm-B) (SmB) |
Saccharomyces cerevisiae | 6g90_b | P40018 | 95.60 | 9.60E-05 | 1.10E-08 | 69.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | TIAL1 |
Nucleolysin TIAR (TIA-1-related protein) |
Homo sapiens | Ulcerative Blepharitis,Spinal Muscular Atrophy,Salpingitis Isthmica Nodosa |
1x4g_a | Q01085 | ENSG00000151923 | TIAL1 | 95.10 | 0.00026 | 3.40E-08 | 53.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.50 | 0.00012 | 1.50E-08 | 65.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | Rbm12 |
RNA-binding protein 12 (RNA-binding motif protein 12) (SH3/WW domain anchor protein in the nucleus) (SWAN) |
Mus musculus | 2cqp_a | Q8R4X3 | 96.10 | 2.30E-05 | 2.90E-09 | 58.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 4.90E-05 | 6.70E-09 | 62.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.30 | 0.00015 | 2.00E-08 | 51.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 4.00E-05 | 5.50E-09 | 62.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | RBM5 H37 LUCA15 |
RNA-binding protein 5 (Protein G15) (Putative tumor suppressor LUCA15) (RNA-binding motif protein 5) (Renal carcinoma antigen NY-REN-9) |
Homo sapiens | Lung Cancer |
2lk1_a | P52756 | ENSG00000003756 | RBM5 | 95.10 | 0.00025 | 2.90E-08 | 44.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | Tc00.1047053511727.270 |
Tc00.1047053511727.270 |
Trypanosoma cruzi | 5opt_h | Q4DY32 | 95.00 | 0.00033 | 3.90E-08 | 63.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | RBM41 |
RNA-binding protein 41 (RNA-binding motif protein 41) |
Homo sapiens | 2cpx_a | Q96IZ5 | ENSG00000089682 | RBM41 | 95.60 | 9.50E-05 | 1.20E-08 | 56.70 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.00 | 3.50E-05 | 4.80E-09 | 62.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.90 | 4.80E-05 | 5.90E-09 | 61.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | NAB3 HMD1 YPL190C |
Nuclear polyadenylated RNA-binding protein 3 |
Saccharomyces cerevisiae | 2kvi_a | P38996 | 95.50 | 0.00011 | 1.30E-08 | 55.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | NAM8 MRE2 YHR086W |
Protein NAM8 |
Saccharomyces cerevisiae | 5zwn_v | Q00539 | 95.40 | 0.00015 | 1.70E-08 | 73.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.80 | 5.50E-05 | 7.50E-09 | 54.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | RAVER1 KIAA1978 |
Ribonucleoprotein PTB-binding 1 (Protein raver-1) |
Homo sapiens | 3h2v_e | Q8IY67 | ENSG00000161847 | RAVER1 | 95.40 | 0.00013 | 1.70E-08 | 50.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YDL167C | NRP1 | SGDID:S000002326 | LARP6 |
La-related protein 6 (Acheron) (Achn) (La ribonucleoprotein domain family member 6) |
Homo sapiens | Brittle Bone Disorder |
2mtg_a | Q9BRS8 | ENSG00000166173 | LARP6 | 96.20 | 2.40E-05 | 2.40E-09 | 66.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 |
2hyi_b | Q9Y5S9 | ENSG00000265241 | RBM8A | 95.10 | 0.00024 | 3.40E-08 | 49.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.70 | 6.70E-05 | 8.50E-09 | 57.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.10 | 2.20E-05 | 3.10E-09 | 61.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.50 | 0.00011 | 1.40E-08 | 56.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.40 | 1.10E-05 | 1.40E-09 | 60.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.10 | 0.00023 | 3.20E-08 | 49.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | ZRANB1 TRABID |
Ubiquitin thioesterase ZRANB1 (EC 3.4.19.12) (TRAF-binding domain-containing protein) (hTrabid) (Zinc finger Ran-binding domain-containing protein 1) |
3.4.19.12 | Homo sapiens | 5af6_g | Q9UGI0 | ENSG00000019995 | ZRANB1 | 95.30 | 0.00021 | 2.30E-08 | 47.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.20 | 1.70E-05 | 2.20E-09 | 69.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.60 | 0.0001 | 1.20E-08 | 58.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 96.00 | 3.20E-05 | 4.00E-09 | 68.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 |
4iuf_a | Q13148 | ENSG00000120948 | TARDBP | 95.10 | 0.00022 | 3.00E-08 | 48.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.20 | 0.00018 | 2.50E-08 | 50.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | HRP1 NAB4 NAB5 YOL123W |
Nuclear polyadenylated RNA-binding protein 4 (Cleavage factor IB) (CFIB) |
Saccharomyces cerevisiae | 2cjk_a | Q99383 | 95.90 | 3.60E-05 | 5.00E-09 | 60.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | 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 | 95.60 | 0.0001 | 1.30E-08 | 56.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | mec-8 CELE_F46A9.6 F46A9.6 |
mec-8 CELE_F46A9.6 F46A9.6 |
Caenorhabditis elegans | 5tkz_b | G5ECJ4 | 95.60 | 8.60E-05 | 1.10E-08 | 54.70 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | ||||
YDL167C | NRP1 | SGDID:S000002326 | EIF4B |
Eukaryotic translation initiation factor 4B (eIF-4B) |
Homo sapiens | Mouth Disease |
2j76_e | P23588 | ENSG00000063046 | EIF4B | 95.70 | 7.10E-05 | 8.50E-09 | 58.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL167C | NRP1 | SGDID:S000002326 | Nup153 |
Nuclear pore complex protein Nup153 (153 kDa nucleoporin) (Nucleoporin Nup153) |
Rattus norvegicus | 3gj7_d | P49791 | 96.60 | 4.10E-06 | 5.00E-10 | 64.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |