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Protein Coding Gene : Abi3bp ABI family member 3 binding protein

Primary Identifier  MGI:2444583 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  320712
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables collagen binding activity and heparin binding activity. Involved in negative regulation of cell population proliferation; negative regulation of connective tissue replacement involved in inflammatory response wound healing; and positive regulation of cardiocyte differentiation. Acts upstream of or within extracellular matrix organization and positive regulation of cell-substrate adhesion. Located in interstitial matrix. Is expressed in several structures, including connective tissue; embryo mesenchyme; gut; male reproductive gland or organ; and olfactory epithelium. Orthologous to human ABI3BP (ABI family member 3 binding protein).
PHENOTYPE: Homozygotes for a null allele show no major changes in anxiety, depression-like behavior, olfactory function or tumor incidence. Homozygotes for a different null allele show reduced cardiac progenitor cell (CPC) differentiation, increased CPC proliferation, and susceptibility to myocardial injury. [provided by MGI curators]
  • synonyms:
  • ABI family member 3 binding protein,
  • MGI:2668157,
  • RIKEN cDNA D930038M13 gene,
  • eratin,
  • TARSH,
  • expressed sequence BG172926,
  • RIKEN cDNA 5033411B22 gene,
  • expressed sequence AI506287,
  • MGI:2146450,
  • D930038M13Rik,
  • 5033411B22Rik,
  • Abi3bp,
  • AI506287,
  • BG172926

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