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Protein Coding Gene : Slc9a8 solute carrier family 9 (sodium/hydrogen exchanger), member 8

Primary Identifier  MGI:1924281 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  77031
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. Involved in acrosome assembly and regulation of intracellular pH. Located in acrosomal vesicle and apical plasma membrane. Is expressed in several structures, including alimentary system; heart; metanephros; nervous system; and respiratory system. Orthologous to human SLC9A8 (solute carrier family 9 member A8).
PHENOTYPE: Homozygotes for a null allele show male sterility, impaired mucin synthesis and bicarbonate secretion in the colon and elongation of the small intestine, cecum and ileum crypts. Homozygotes for another null allele show male sterility, asthenospermia, globozoospermia, and abnormal acrosome assembly. [provided by MGI curators]
  • synonyms:
  • expressed sequence AI182282,
  • 1200006P13Rik,
  • MGI:1923489,
  • RIKEN cDNA 6430709P13 gene,
  • Slc9a8,
  • RIKEN cDNA 1200006P13 gene,
  • AI182282,
  • 6430709P13Rik,
  • solute carrier family 9 (sodium/hydrogen exchanger), member 8,
  • MGI:2138851,
  • NHE8

Features --> Cross References

Genome

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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

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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