Homo sapiens Gene: SYT14
Summary
InnateDB Gene IDBG-106460.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SYT14
Gene Name synaptotagmin XIV
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000143469
Encoded Proteins
synaptotagmin XIV
synaptotagmin XIV
synaptotagmin XIV
synaptotagmin XIV
synaptotagmin XIV
synaptotagmin XIV
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1;3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:209938174-210171315
Strand Forward strand
Band q32.2
Transcripts
ENST00000367019 ENSP00000355986
ENST00000367015 ENSP00000355982
ENST00000399639 ENSP00000445837
ENST00000472886 ENSP00000418901
ENST00000534859 ENSP00000442891
ENST00000537238 ENSP00000437423
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0005543 phospholipid binding
GO:0042803 protein homodimerization activity
GO:0046982 protein heterodimerization activity
Biological Process
GO:0008219 cell death
Cellular Component
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.630129 Hs.658866
RefSeq NM_001146261 NM_001146262 NM_001146264 NM_001256006 NM_153262 XM_006711264
HUGO
OMIM
CCDS CCDS31014 CCDS53470 CCDS58058
HPRD 11617
IMGT
EMBL
GenPept
RNA Seq Atlas