Gene Gene information from NCBI Gene database.
Entrez ID 222183
Gene name Serine/arginine repetitive matrix 3
Gene symbol SRRM3
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7q11.23
miRNA miRNA information provided by mirtarbase database.
142
miRTarBase ID miRNA Experiments Reference
MIRT017701 hsa-miR-335-5p Microarray 18185580
MIRT1389887 hsa-miR-1184 CLIP-seq
MIRT1389888 hsa-miR-1193 CLIP-seq
MIRT1389889 hsa-miR-1197 CLIP-seq
MIRT1389890 hsa-miR-1263 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0003729 Function MRNA binding IBA
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
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A6NNA2
Protein name Serine/arginine repetitive matrix protein 3
Protein function May play a role in regulating breast cancer cell invasiveness (PubMed:26053433). May be involved in RYBP-mediated breast cancer progression (PubMed:27748911).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08312 cwf21 55 98 cwf21 domain Domain
PF15230 SRRM_C 522 582 Serine/arginine repetitive matrix protein C-terminus Family
Tissue specificity TISSUE SPECIFICITY: Expressed in breast cancer cell lines. {ECO:0000269|PubMed:26053433}.
Sequence
MSSTVNNGAASMQSTPDAANGFPQPSSSSGTWPRAEEELRAAEPGLVKRAHREILDHERK
RRVELKCMELQEMMEEQGYSEEEIRQKVGTFRQMLMEK
EGVLTREDRPGGHIVAETPRLT
EGAEPGLEYAPFDDDDGPVDCDCPASCYRGHRGYRTKHWSSSSASPPPKKKKKKKGGHRR
SRKKRRLESECSCGSSSPLRKKKKSVKKHRRDRSDSGSRRKRRHRSRSSKCKRKEKNKEK
KRPHTESPGRRSHRHSSGSSHSPSLSSHYSDSRSPSRLSPKHRDEGRKTGSQRSSGSRSP
SPSGGSGWGSPQRNGGSGQRSGAHGGRPGSAHSPPDKPSSPSPRVRDKAAAAAPTPPARG
KESPSPRSAPSSQGRGGRAAGGAGRRRRRRRRRRRSRSSASAPRRRGRRRPRPAPPRGSS
RSLSRARSSSDSGSGRGAPGPGPEPGSERGHGGHGKRAKERPPRARPASTSPSPGAHGRR
GGPEGKSSSRSPGPHPRSWSSSRSPSKSRSRSAEKRPHSPSRSPSPKKPLSRDKDGEGRA
RHSEAEATRARRRSRSYSPIRKRRRDSPSFMEPRRITSAASV
LFHTTGPAPLPPPAA
Sequence length 597
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ASTROCYTOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Neoplasms Associate 34312180
★☆☆☆☆
Found in Text Mining only
Periodontitis Associate 35397550
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Associate 34312180
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Castration Resistant Associate 34312180
★☆☆☆☆
Found in Text Mining only