Entity Details

Primary name SLC9A9
Entity type gene
Source Source Link

Details

PrimaryID285195
RefseqGeneNG_017077
SymbolSLC9A9
Namesolute carrier family 9 member A9
Chromosome3
Location3q24
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-12-14
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSL9A9_HUMAN

GO terms

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GOName
GO:0005886 plasma membrane
GO:0006811 ion transport
GO:0015385 sodium:proton antiporter activity
GO:0015386 potassium:proton antiporter activity
GO:0016021 integral component of membrane
GO:0031902 late endosome membrane
GO:0051453 regulation of intracellular pH
GO:0055037 recycling endosome
GO:0071805 potassium ion transmembrane transport
GO:0098719 sodium ion import across plasma membrane

Diseases

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Disease IDSourceNameDescription
613410 OMIMAutism 16 (AUTS16)A complex multifactorial, pervasive developmental disorder characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Most individuals with autism also manifest moderate mental retardation. AUTS16 can be associated with epilepsy. Disease susceptibility is associated with variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
SLC9A9ZDHHC17BioGRID, IntAct24705354 details
SLC9A9OPRM1BioGRID, MINT28298427 details
SLC9A9TP53BioGRID27229929 details