Entity Details

Primary name SYT14
Entity type gene
Source Source Link

Details

PrimaryID255928
RefseqGeneNG_031962
SymbolSYT14
Namesynaptotagmin 14
Chromosome1
Location1q32.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-07-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSYT14_HUMAN

GO terms

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GOName
GO:0016021 integral component of membrane

Diseases

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Disease IDSourceNameDescription
614229 OMIMSpinocerebellar ataxia, autosomal recessive, 11 (SCAR11)A form of spinocerebellar ataxia, a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR11 is associated with psychomotor retardation. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
SYT14SYT16BioGRID, HPRD12801916 details
SYT14SYT14HPRD12801916 details