Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6769
Gene name Gene Name - the full gene name approved by the HGNC.
SH3 and cysteine rich domain
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STAC
Synonyms (NCBI Gene) Gene synonyms aliases
STAC1
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p22.3-p22.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT719332 hsa-miR-4502 HITS-CLIP 19536157
MIRT719331 hsa-miR-204-3p HITS-CLIP 19536157
MIRT719330 hsa-miR-4646-5p HITS-CLIP 19536157
MIRT719329 hsa-miR-6828-5p HITS-CLIP 19536157
MIRT719328 hsa-miR-4505 HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003009 Process Skeletal muscle contraction IBA 21873635
GO:0005515 Function Protein binding IPI 16260042, 21812934, 28514442, 32296183, 32814053
GO:0005829 Component Cytosol NAS 8954993
GO:0007165 Process Signal transduction NAS 8954993
GO:0030315 Component T-tubule IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602317 11353 ENSG00000144681
Protein
UniProt ID Q99469
Protein name SH3 and cysteine-rich domain-containing protein (Src homology 3 and cysteine-rich domain-containing protein)
Protein function Promotes expression of the ion channel CACNA1H at the cell membrane, and thereby contributes to the regulation of channel activity. Plays a minor and redundant role in promoting the expression of calcium channel CACNA1S at the cell membrane, and
PDB 2DL4 , 6B25
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00130 C1_1 108 162 Phorbol esters/diacylglycerol binding domain (C1 domain) Domain
PF16664 STAC2_u1 165 287 Disordered
PF14604 SH3_9 292 340 Variant SH3 domain Domain
Sequence
MIPPSSPREDGVDGLPKEAVGAEQPPSPASTSSQESKLQKLKRSLSFKTKSLRSKSADNF
FQRTNSEDMKLQAHMVAEISPSSSPLPAPGSLTSTPARAGLHPGGKAHAFQEYIFKKPTF
CDVCNHMIVGTNAKHGLRCKACKMSIHHKCTDGLAPQRCMGK
LPKGFRRYYSSPLLIHEQ
FGCIKEVMPIACGNKVDPVYETLRFGTSLAQRTKKGSSGSGSDSPHRTSTSDLVEVPEEA
NGPGGGYDLRKRSNSVFTYPENGTDDFRDPAKNINHQGSLSKDPLQM
NTYVALYKFVPQE
NEDLEMRPGDIITLLEDSNEDWWKGKIQDRIGFFPANFVQ
RLQQNEKIFRCVRTFIGCKE
QGQITLKENQICVSSEEEQDGFIRVLSGKKKGLIPLDVLENI
Sequence length 402
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Dermatitis Dermatitis, Allergic Contact rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 16033404
Unknown
Disease term Disease name Evidence References Source
Celiac disease Celiac disease GWAS
Asthma Asthma GWAS