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Protein Coding Gene : Slc9a7 solute carrier family 9 (sodium/hydrogen exchanger), member 7
Primary Identifier  MGI:2444530 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  236727
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable potassium:proton antiporter activity and sodium:proton antiporter activity. Predicted to be involved in potassium ion transmembrane transport; regulation of Golgi lumen acidification; and sodium ion import across plasma membrane. Predicted to act upstream of or within potassium ion transport and sodium ion transport. Predicted to be located in recycling endosome membrane and trans-Golgi network. Predicted to be active in plasma membrane and recycling endosome. Human ortholog(s) of this gene implicated in X-linked intellectual developmental disorder 108. Orthologous to human SLC9A7 (solute carrier family 9 member A7).
  • synonyms:
  • NHE7,
  • RIKEN cDNA A530087D17 gene,
  • solute carrier family 9 (sodium/hydrogen exchanger), member 7,
  • Slc9a7,
  • A530087D17Rik
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0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

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Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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