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Protein Coding Gene : Ppm1f protein phosphatase 1F (PP2C domain containing)

Primary Identifier  MGI:1918464 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  68606
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable calmodulin-dependent protein phosphatase activity and protein tyrosine/serine/threonine phosphatase activity. Predicted to be involved in several processes, including negative regulation of cell-cell adhesion mediated by cadherin; positive regulation of cellular component biogenesis; and regulation of gene expression. Predicted to act upstream of or within apoptotic process. Predicted to be located in perinuclear region of cytoplasm. Predicted to be part of protein-containing complex. Predicted to be active in cytosol and nucleus. Is expressed in several structures, including alimentary system; central nervous system; eye; genitourinary system; and respiratory system. Orthologous to human PPM1F (protein phosphatase, Mg2+/Mn2+ dependent 1F).
PHENOTYPE: Mice homozygous for a targeted mutation are not detected at weaning. Mice heterozygous for a targeted mutation display hyperactivity and an increase in pain threshold. [provided by MGI curators]
  • synonyms:
  • 4933427B07Rik,
  • RIKEN cDNA 4933427B07 gene,
  • RIKEN cDNA 1110021B16 gene,
  • MGI:1915856,
  • protein phosphatase 1F (PP2C domain containing),
  • MGC:25978,
  • 1110021B16Rik,
  • Ppm1f,
  • mKIAA0015

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