Gene Gene information from NCBI Gene database.
Entrez ID 51760
Gene name Synaptotagmin 17
Gene symbol SYT17
Synonyms (NCBI Gene)
Syt-17sytXVII
Chromosome 16
Chromosome location 16p12.3
miRNA miRNA information provided by mirtarbase database.
227
miRTarBase ID miRNA Experiments Reference
MIRT018929 hsa-miR-335-5p Microarray 18185580
MIRT607313 hsa-miR-8485 HITS-CLIP 22927820
MIRT663407 hsa-miR-329-3p HITS-CLIP 22927820
MIRT663406 hsa-miR-362-3p HITS-CLIP 22927820
MIRT607312 hsa-miR-603 HITS-CLIP 22927820
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0000149 Function SNARE binding IBA
GO:0005515 Function Protein binding IPI 16189514, 16730941, 25416956, 28514442, 31515488, 32296183
GO:0005544 Function Calcium-dependent phospholipid binding IBA
GO:0005802 Component Trans-Golgi network IEA
GO:0005886 Component Plasma membrane IBA
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.
Q9BSW7
Protein name Synaptotagmin-17 (Protein B/K) (Synaptotagmin XVII) (SytXVII)
Protein function Plays a role in dendrite formation by melanocytes (PubMed:23999003).
PDB 2ENP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 199 312 C2 domain Domain
PF00168 C2 336 443 C2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed abundantly in brain (frontal and temporal lobes, hippocampus, hypothalamus, amygdala, substantia nigra, and pituitary), kidney, and prostate. Expressed in fetal brain, kidney and lung (PubMed:16672768). Expressed in melanocyt
Sequence
MAYIQLEPLNEGFLSRISGLLLCRWTCRHCCQKCYESSCCQSSEDEVEILGPFPAQTPPW
LMASRSSDKDGDSVHTASEVPLTPRTNSPDGRRSSSDTSKSTYSLTRRISSLESRRPSSP
LIDIKPIEFGVLSAKKEPIQPSVLRRTYNPDDYFRKFEPHLYSLDSNSDDVDSLTDEEIL
SKYQLGMLHFSTQYDLLHNHLTVRVIEARDLPPPISHDGSRQDMAHSNPYVKICLLPDQK
NSKQTGVKRKTQKPVFEERYTFEIPFLEAQRRTLLLTVVDFDKFSRHCVIGKVSVPLCEV
DLVKGGHWWKAL
IPSSQNEVELGELLLSLNYLPSAGRLNVDVIRAKQLLQTDVSQGSDPF
VKIQLVHGLKLVKTKKTSFLRGTIDPFYNESFSFKVPQEELENASLVFTVFGHNMKSSND
FIGRIVIGQYSSGPSETNHWRRM
LNTHRTAVEQWHSLRSRAECDRVSPASLEVT
Sequence length 474
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
CORNEAL ASTIGMATISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PARKINSON DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Autoimmune Diseases of the Nervous System Stimulate 32369831
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 34127544
★☆☆☆☆
Found in Text Mining only