solute carrier family 9 member A7

Summary
Gene Symbol
  • SLC9A7
Organism
Homo sapiens (human)
NCBI Gene
84679
PubChem
84679
Alliance of Genome Resources
Annotation
Keyword
  • Antiport
  • Cell membrane
  • Disease variant
  • Endosome
  • Glycoprotein
  • Golgi apparatus
  • Intellectual disability
  • Phosphoprotein
  • Potassium transport
  • Proteomics identification
  • Reference proteome
  • Signal
  • Sodium transport
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q96T83
  • Na(+)/H(+) exchanger 7
  • Solute carrier family 9 member 7
A0A087WXD1
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
sodium/hydrogen exchanger
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0111844 X-linked intellectual developmental disorder 108

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024