Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6860
Gene name Gene Name - the full gene name approved by the HGNC.
Synaptotagmin 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SYT4
Synonyms (NCBI Gene) Gene synonyms aliases
HsT1192
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q12.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT020421 hsa-miR-106b-5p Microarray 17242205
MIRT021609 hsa-miR-142-3p Microarray 17612493
MIRT038996 hsa-let-7b-3p CLASH 23622248
MIRT532102 hsa-miR-548m PAR-CLIP 22012620
MIRT532101 hsa-miR-3129-3p PAR-CLIP 22012620
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 16189514, 25416956, 32296183
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
600103 11512 ENSG00000132872
Protein
UniProt ID Q9H2B2
Protein name Synaptotagmin-4 (Synaptotagmin IV) (SytIV)
Protein function Synaptotagmin family member which does not bind Ca(2+) (By similarity) (PubMed:23999003). Involved in neuronal dense core vesicles (DCVs) mobility through its interaction with KIF1A. Upon increased neuronal activity, phosphorylation by MAPK8/JNK
PDB 1UGK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00168 C2 168 274 C2 domain Domain
PF00168 C2 302 408 C2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in melanocytes (PubMed:23999003). Expressed in brain. Within brain, expression is highest in hippocampus, with substantial levels also detected in amygdala and thalamus (PubMed:23999003). {ECO:0000269|PubMed:23999003}.
Sequence
MAPITTSREEFDEIPTVVGIFSAFGLVFTVSLFAWICCQRKSSKSNKTPPYKFVHVLKGV
DIYPENLNSKKKFGADDKNEVKNKPAVPKNSLHLDLEKRDLNGNFPKTNLKPGSPSDLEN
ATPKLFLEGEKESVSPESLKSSTSLTSEEKQEKLGTLFFSLEYNFERKAFVVNIKEARGL
PAMDEQSMTSDPYIKMTILPEKKHKVKTRVLRKTLDPAFDETFTFYGIPYTQIQELALHF
TILSFDRFSRDDIIGEVLIPLSGIELSEGKMLMN
REIIKRNVRKSSGRGELLISLCYQST
TNTLTVVVLKARHLPKSDVSGLSDPYVKVNLYHAKKRISKKKTHVKKCTPNAVFNELFVF
DIPCEGLEDISVEFLVLDSERGSRNEVIGQLVLGAAAEGTGGEHWKEI
CDYPRRQIAKWH
VLCDG
Sequence length 425
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Melanoma melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
21499247
Unknown
Disease term Disease name Evidence References Source
Seborrheic dermatitis Seborrheic dermatitis GWAS
Diabetes Diabetes GWAS
Mental Depression Mental Depression GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Associations from Text Mining
Disease Name Relationship Type References
Diabetes Mellitus Type 2 Associate 26337083
Stomach Neoplasms Associate 34229539