Gene Gene information from NCBI Gene database.
Entrez ID 57035
Gene name Arginine and serine rich protein 1
Gene symbol RSRP1
Synonyms (NCBI Gene)
C1orf63NPD014
Chromosome 1
Chromosome location 1p36.11
miRNA miRNA information provided by mirtarbase database.
128
miRTarBase ID miRNA Experiments Reference
MIRT441058 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT441057 hsa-miR-20a-5p HITS-CLIP 22473208
MIRT441058 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT728120 hsa-miR-17-5p HITS-CLIP 22473208
MIRT728119 hsa-miR-20b-5p HITS-CLIP 22473208
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0000245 Process Spliceosomal complex assembly IDA 34042961
GO:0005515 Function Protein binding IPI 16189514, 25416956, 31515488, 32296183, 33961781
GO:0005634 Component Nucleus IDA 34042961
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620030 25234 ENSG00000117616
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BUV0
Protein name Arginine/serine-rich protein 1
Protein function Probably acts as a spliceosomal factor that contributes to spliceosome assembly and regulates the isoform switching of proteins such as PARP6.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17069 RSRP 1 290 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain (at protein level). {ECO:0000269|PubMed:34042961}.
Sequence
Sequence length 290
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANTI-D ISOIMMUNIZATION AFFECTING PREGNANCY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14 Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEMOLYTIC DISEASE OF FETUS AND NEWBORN, RH-INDUCED Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEMOLYTIC DISEASE OF FETUS OR NEWBORN DUE TO RHD ISOIMMUNIZATION Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 26209438
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 26209438
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 26209438
★☆☆☆☆
Found in Text Mining only
Carcinoma Ovarian Epithelial Associate 23551967
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 26209438
★☆☆☆☆
Found in Text Mining only