Gene Gene information from NCBI Gene database.
Entrez ID 400745
Gene name SH2 domain containing 5
Gene symbol SH2D5
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1p36.12
miRNA miRNA information provided by mirtarbase database.
103
miRTarBase ID miRNA Experiments Reference
MIRT717237 hsa-miR-4750-3p HITS-CLIP 19536157
MIRT717236 hsa-miR-93-3p HITS-CLIP 19536157
MIRT717235 hsa-miR-3692-5p HITS-CLIP 19536157
MIRT717234 hsa-miR-6859-3p HITS-CLIP 19536157
MIRT717233 hsa-miR-6846-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25331951
GO:0014069 Component Postsynaptic density IBA
GO:0014069 Component Postsynaptic density IEA
GO:0014069 Component Postsynaptic density ISS
GO:0045202 Component Synapse 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.
Q6ZV89
Protein name SH2 domain-containing protein 5
Protein function May be involved in synaptic plasticity regulation through the control of Rac-GTP levels.
Family and domains
Sequence
MQKAGAGGRRASDCGLAPHRPRCITKFAQYVGSFPVDDLDTQESVWLVQQQLWALKDCPR
RRAVILKFSLQGLKIYSGEGEVLLMAHALRRILYSTWCPADCQFAFMARNPRSPASKLFC
HLFVGSQPGEVQILHLLLCRSFQLAYLLQHPEERAQPEPCPGPTGEVPLKPLSSSGGLVR
EPFGRDQLSQNVHALVSFRRLPAEGLVGSGKELPESEGRARHARLGNPYCSPTLVRKKAI
RSKVIRSGAYRGCTYETQLQLSAREAFPAAWEAWPRGPGGHSCLVESEGSLTENIWAFAG
ISRPCALALLRRDVLGAFLLWPELGASGQWCLSVRTQCGVVPHQVFRNHLGRYCLEHLPA
EFPSLEALVENHAVTERSLFCPLDMGRLNPTYEEQDCGPPGRPPRTLRPLSHAKSEAELQ
GLG
Sequence length 423
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
STOMACH DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 30659097 Stimulate
★☆☆☆☆
Found in Text Mining only
Hepatitis B Hepatitis b Pubtator 30659097 Stimulate
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 30659097
★☆☆☆☆
Found in Text Mining only
Liver neoplasms Liver neoplasms BEFREE 30659097
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Lung neoplasms Pubtator 37187527 Associate
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma BEFREE 25331951
★☆☆☆☆
Found in Text Mining only