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Allele : Fancl<gcd> Fanconi anemia, complementation group L; germ cell deficient

Primary Identifier  MGI:1861640 Allele Type  Transgenic
Gene  Fancl Inheritance Mode  Recessive
Strain of Origin  (CBA/J x C57BL/6J)F2 Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation was identified as a transgene insertion that also deletes approximately 150 kb of genomic sequence at the insertion site. This deletion removes exons 4-14 of Fancl and also removes exons 2-11 of a neighboring gene Vrk2. The transgene contains a fragment of goat DNA. A transgene expressing Vrk2 that was introduced into homozygous mice failed to rescue the phenotype, suggesting that the deletion of Fancl was solely responsible for the phenotype seen in these mice.
  • mutations:
  • Intergenic deletion,
  • Insertion
  • synonyms:
  • Phf9<gcd>,
  • Phf9<gcd>,
  • gcd,
  • gcd
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

7 Publication categories

Trail: Allele