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Protein Coding Gene : Fance Fanconi anemia, complementation group E
Primary Identifier  MGI:1920025 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  72775
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 9.1.0)

Acts upstream of or within several processes, including cell maturation; gonad development; and spermatogenesis. Is active in nuclear periphery. Is expressed in central nervous system; liver; metanephros; and retina. Human ortholog(s) of this gene implicated in Fanconi anemia complementation group E. Orthologous to human FANCE (FA complementation group E).
PHENOTYPE: Homozygous knockout causes reduced male fertility. [provided by MGI curators]
  • synonyms:
  • 2810451D06Rik,
  • MGI:2146848,
  • AI415634,
  • Fance,
  • RIKEN cDNA 2810451D06 gene,
  • Fanconi anemia, complementation group E,
  • expressed sequence AW209126,
  • AW209126,
  • expressed sequence AI415634,
  • MGI:2147054
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Canonical gene --> Exons in specific strains

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Phenotype

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Disease

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