Entity Details

Primary name SLC9A7
Entity type gene
Source Source Link

Details

PrimaryID84679
RefseqGeneNG_012622
SymbolSLC9A7
Namesolute carrier family 9 member A7
ChromosomeX
LocationXp11.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-26
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSL9A7_HUMAN

GO terms

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GOName
GO:0000139 Golgi membrane
GO:0005802 trans-Golgi network
GO:0005886 plasma membrane
GO:0006811 ion transport
GO:0006885 regulation of pH
GO:0015385 sodium:proton antiporter activity
GO:0015386 potassium:proton antiporter activity
GO:0016021 integral component of membrane
GO:0043231 intracellular membrane-bounded organelle
GO:0051453 regulation of intracellular pH
GO:0055037 recycling endosome
GO:0055038 recycling endosome membrane
GO:0071805 potassium ion transmembrane transport
GO:0098719 sodium ion import across plasma membrane
GO:1905526 regulation of Golgi lumen acidification

Diseases

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Disease IDSourceNameDescription
301024 OMIMIntellectual developmental disorder, X-linked 108 (MRX108)A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions