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Protein Coding Gene : Nherf2 NHERF family PDZ scaffold protein 2

Primary Identifier  MGI:1890662 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  65962
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables phosphatase binding activity. Acts upstream of or within negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction and sensory perception of sound. Located in several cellular components, including apical plasma membrane; nucleus; and stereocilium. Is expressed in atrioventricular valve; cochlea epithelium; organ of Corti; and semilunar valve. Orthologous to human NHERF2 (NHERF family PDZ scaffold protein 2).
PHENOTYPE: Mice homozygous for a null allele are viable, fertile and overtly normal and display normal cAMP- and cGMP-activated CFTR transepithelial chloride transport and bicarbonate secretion in the small intestine. [provided by MGI curators]
  • synonyms:
  • solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 2,
  • Tka-1,
  • E3karp,
  • Slc9a3r2,
  • Sry interacting protein 1,
  • 1200011K07Rik,
  • 2010007A20Rik,
  • RIKEN cDNA 2010007A20 gene,
  • Sip-1,
  • MGI:2178113,
  • MGI:1915601,
  • MGI:1915060,
  • RIKEN cDNA 1200011K07 gene,
  • NHERF family PDZ scaffold protein 2,
  • MGI:1923770,
  • Sryip1,
  • 0610011L07Rik,
  • Nherf2,
  • Sip1,
  • Octs2,
  • RIKEN cDNA 0610011L07 gene

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