Gene Gene information from NCBI Gene database.
Entrez ID 57586
Gene name Synaptotagmin 13
Gene symbol SYT13
Synonyms (NCBI Gene)
-
Chromosome 11
Chromosome location 11p11.2
Summary This gene encodes a member of the large synaptotagmin protein family. Family members have an extracellular N-terminal transmembrane domain and a cytoplasmic C terminus with two tandem C2 domains (C2A and C2B). Synaptotogmin family members can form homo- a
miRNA miRNA information provided by mirtarbase database.
260
miRTarBase ID miRNA Experiments Reference
MIRT712055 hsa-miR-4688 HITS-CLIP 19536157
MIRT712054 hsa-miR-6743-5p HITS-CLIP 19536157
MIRT712053 hsa-miR-6798-5p HITS-CLIP 19536157
MIRT712052 hsa-miR-4775 HITS-CLIP 19536157
MIRT439494 hsa-miR-382-5p HITS-CLIP 24374217
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0000149 Function SNARE binding IBA
GO:0005544 Function Calcium-dependent phospholipid binding IBA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607716 14962 ENSG00000019505
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7L8C5
Protein name Synaptotagmin-13 (Synaptotagmin XIII) (SytXIII)
Protein function May be involved in transport vesicle docking to the plasma membrane.
PDB 1WFM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 171 277 C2 domain Domain
PF00168 C2 302 410 C2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, pancreas and kidney. {ECO:0000269|PubMed:11543631}.
Sequence
MVLSVPVIALGATLGTATSILALCGVTCLCRHMHPKKGLLPRDQDPDLEKAKPSLLGSAQ
QFNVKKSTEPVQPRALLKFPDIYGPRPAVTAPEVINYADYSLRSTEEPTAPASPQPPNDS
RLKRQVTEELFILPQNGVVEDVCVMETWNPEKAASWNQAPKLHYCLDYDCQKAELFVTRL
EAVTSNHDGGCDCYVQGSVANRTGSVEAQTALKKRQLHTTWEEGLVLPLAEEELPTATLT
LTLRTCDRFSRHSVAGELRLGLDGTSVPLGAAQWGEL
KTSAKEPSAGAGEVLLSISYLPA
ANRLLVVLIKAKNLHSNQSKELLGKDVSVKVTLKHQARKLKKKQTKRAKHKINPVWNEMI
MFELPDDLLQASSVELEVLGQDDSGQSCALGHCSLGLHTSGSERSHWEEM
LKNPRRQIAM
WHQLHL
Sequence length 426
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
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Atrial Fibrillation Associate 37960721
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 34677264
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 29154080
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 34677264
★☆☆☆☆
Found in Text Mining only
Neuroendocrine Tumors Associate 29154080
★☆☆☆☆
Found in Text Mining only