Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84258
Gene name Gene Name - the full gene name approved by the HGNC.
Synaptotagmin 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SYT3
Synonyms (NCBI Gene) Gene synonyms aliases
SytIII
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2122133 hsa-miR-128 CLIP-seq
MIRT2122134 hsa-miR-15a CLIP-seq
MIRT2122135 hsa-miR-15b CLIP-seq
MIRT2122136 hsa-miR-16 CLIP-seq
MIRT2122137 hsa-miR-195 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000149 Function SNARE binding IBA 21873635
GO:0001786 Function Phosphatidylserine binding IBA 21873635
GO:0005509 Function Calcium ion binding IBA 21873635
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0005544 Function Calcium-dependent phospholipid binding IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600327 11511 ENSG00000213023
Protein
UniProt ID Q9BQG1
Protein name Synaptotagmin-3 (Synaptotagmin III) (SytIII)
Protein function Ca(2+) sensor involved in Ca(2+)-dependent exocytosis of secretory vesicles through Ca(2+) and phospholipid binding to the C2 domain. Ca(2+) induces binding of the C2-domains to phospholipid membranes and to assembled SNARE-complexes; both actio
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 314 421 C2 domain Domain
PF00168 C2 446 553 C2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in melanocytes (PubMed:23999003). {ECO:0000269|PubMed:23999003}.
Sequence
MSGDYEDDLCRRALILVSDLCARVRDADTNDRCQEFNDRIRGYPRGPDADISVSLLSVIV
TFCGIVLLGVSLFVSWKLCWVPWRDKGGSAVGGGPLRKDLGPGVGLAGLVGGGGHHLAAG
LGGHPLLGGPHHHAHAAHHPPFAELLEPGSLGGSDTPEPSYLDMDSYPEAAAAAVAAGVK
PSQTSPELPSEGGAGSGLLLLPPSGGGLPSAQSHQQVTSLAPTTRYPALPRPLTQQTLTS
QPDPSSEERPPALPLPLPGGEEKAKLIGQIKPELYQGTGPGGRRSGGGPGSGEAGTGAPC
GRISFALRYLYGSDQLVVRILQALDLPAKDSNGFSDPYVKIYLLPDRKKKFQTKVHRKTL
NPVFNETFQFSVPLAELAQRKLHFSVYDFDRFSRHDLIGQVVLDNLLELAEQPPDRPLWR
D
IVEGGSEKADLGELNFSLCYLPTAGRLTVTIIKASNLKAMDLTGFSDPYVKASLISEGR
RLKKRKTSIKKNTLNPTYNEALVFDVAPESVENVGLSIAVVDYDCIGHNEVIGVCRVGPD
AADPHGREHWAEM
LANPRKPVEHWHQLVEEKTVTSFTKGSKGLSEKENSE
Sequence length 590
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
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