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Allele : Hsdr1 hepatocyte specific developmental regulation 1

Primary Identifier  MGI:1856906 Allele Type  Radiation induced
Gene  Hsdr1 Inheritance Mode  Recessive
Strain of Origin  STOCK Del(7)Tyr<c-3H> and Tyr<c-14CoS> Is Recombinase  false
Is Wild Type  false
description  A number of radiation-induced deletions overlap at the albino (Tyr, tyrosinase) locus. References J:5437 and J:6158 describe the albino deletions that identified Hsdr1, Del(7)Tyr and Tyr. The proximal breakpoint of the Tyrc-14Cos, deletion disrupts the gene Fah, encoding the enzyme fumarylacetoacetate hydrolase (EC 3.7.1.2) (J:2947), and it has been argued that the lethal effect of the deletion may result from this disruption, and that Hsdr1 and Fah are identical (J:16987).
  • mutations:
  • Deletion
  • synonyms:
  • alf,
  • alf,
  • albino lethal factor,
  • albino lethal factor
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1 Feature

Trail: Allele

Genome

0 Expresses

1 Mutation Involves

Trail: Allele

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

8 Publication categories

Trail: Allele