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Allele : Fancm<Chaos4> Fanconi anemia, complementation group M; chromosome aberrations occurring spontaneously 4

Primary Identifier  MGI:5704402 Allele Type  Chemically induced (ENU)
Attribute String  Not Specified Gene  Fancm
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  The molecular lesion was identified as a de novo T-to-C transition at nucleotide 524 of the coding region. This point mutation changes a highly conserved cysteine residue to arginine (C142A) that is located within the DEXDc domain of this DEAD-like helicase.
  • mutations:
  • Single point mutation
  • synonyms:
  • Fancm<C4>,
  • Fancm<C4>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

3 Publication categories