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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 8.0.0)

Acts upstream of or within gene expression; homeostasis of number of cells; and ovarian follicle development. Predicted to be located in centrosome; chromatin; and nucleoplasm. Predicted to be part of Fanconi anaemia nuclear complex. 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:
  • AI415634,
  • MGI:2147054,
  • Fance,
  • RIKEN cDNA 2810451D06 gene,
  • expressed sequence AI415634,
  • Fanconi anemia, complementation group E,
  • 2810451D06Rik,
  • MGI:2146848,
  • AW209126,
  • expressed sequence AW209126
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Features --> Cross References

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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.

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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