Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
149563
Gene name Gene Name - the full gene name approved by the HGNC.
Steroid receptor associated and regulated protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SRARP
Synonyms (NCBI Gene) Gene synonyms aliases
C1orf64, ERRF
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.13
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT620005 hsa-miR-1470 HITS-CLIP 23824327
MIRT620003 hsa-miR-1253 HITS-CLIP 23824327
MIRT620002 hsa-miR-6770-5p HITS-CLIP 23824327
MIRT620001 hsa-miR-1911-5p HITS-CLIP 23824327
MIRT620000 hsa-miR-204-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 22341523
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 22341523
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619448 28339 ENSG00000183888
Protein
UniProt ID Q8NEQ6
Protein name Steroid receptor-associated and regulated protein (Estrogen receptor-related factor) (ER-related factor) (Steroid receptor-regulated protein)
Protein function May regulate the transcriptional function of androgen and estrogen receptors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15547 C1ORF64 33 169 Steroid receptor-associated and regulated protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in breast tumors with a higher expression level in estrogen receptor-positive cancers (PubMed:22341523, PubMed:28915724). {ECO:0000269|PubMed:22341523, ECO:0000269|PubMed:28915724}.
Sequence
Sequence length 169
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Heart Failure Heart failure N/A N/A GWAS
Hypertrophic cardiomyopathy Hypertrophic cardiomyopathy N/A N/A GWAS