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Allele : Del(1)3H deletion, Chr 1, Harwell 3
Primary Identifier  MGI:1856175 Allele Type  Radiation induced
Gene  Del(1)3H Inheritance Mode  Semidominant
Strain of Origin  (C3H/HeH x 101/H)F1 Is Recombinase  false
Is Wild Type  false
molecularNote  Maternal X-irradiation produced this a deletion of multiple genes. The distal breakpoint maps to a location within D1mit79 and D1mit134 and a proximal endpoint maps between Tnp1 and Vil.
  • mutations:
  • Intergenic deletion
  • synonyms:
  • retarded splotch,
  • retarded splotch,
  • Sp-3H,
  • Pax3<Sp-r>,
  • Sp-3H,
  • Pax3<Sp-r>
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1 Feature

Genome

0 Expresses

66 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

7 Publication categories





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