Mus musculus Gene: Syt12
Summary
InnateDB Gene IDBG-129615.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Syt12
Gene Name synaptotagmin XII
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000049303
Encoded Proteins
synaptotagmin XII
synaptotagmin XII
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000173227:
This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate calcium-dependent regulation of membrane trafficking in synaptic transmission. Studies of the orthologous gene in rat have shown that the encoded protein selectively modulates spontaneous synaptic-vesicle exocytosis and may also be involved in regulating calcium independent secretion in nonneuronal cells. Alternative splicing results in multiple transcript variants. The gene has previously been referred to as synaptotagmin XI but has been renamed synaptotagmin XII to be standard with mouse and rat official nomenclature.[provided by RefSeq, Apr 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 19:4445908-4477447
Strand Reverse strand
Band A
Transcripts
ENSMUST00000059295 ENSMUSP00000055237
ENSMUST00000128114
ENSMUST00000133222
ENSMUST00000166191 ENSMUSP00000130418
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0005515 protein binding
Biological Process
GO:0006810 transport
Cellular Component
GO:0016021 integral component of membrane
GO:0030054 cell junction
GO:0030672 synaptic vesicle membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q920N7
TrEMBL Q14AG7
UniProt Splice Variant
Entrez Gene 171180
UniGene Mm.262270
RefSeq NM_134164
OMIM
CCDS CCDS29428
HPRD
IMGT
MGI ID MGI:2159601
MGI Symbol Syt12
EMBL AB062804 AK046627 AK083139 BC116846 BC116848 CH466612
GenPept AAI16847 AAI16849 BAB69674 BAC32812 BAC38779 EDL33051
RNA Seq Atlas 171180