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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 8.0.0)

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 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,
  • A530087D17Rik,
  • Slc9a7,
  • RIKEN cDNA A530087D17 gene,
  • solute carrier family 9 (sodium/hydrogen exchanger), member 7
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Features --> Cross References

Genome

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0 Canonical

0 CDSs

0 Exons

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0 Involved In Mutations

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0 Transgenic Expressors

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

Genes --> Homologs

Interactions

4 Pathways

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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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