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Allele : Del(10)1H deletion, Chr 10, Harwell 1

Primary Identifier  MGI:1856365 Allele Type  Radiation induced
Gene  Del(10)1H Inheritance Mode  Semidominant
Strain of Origin  (C3H/HeH x 101/H)F1 Is Recombinase  false
Is Wild Type  false
molecularNote  This X-ray-induced deletion encompasses about 10% of Chr 10, including the Kitl locus (J:5931). Southern analyses of genomic DNA indicate that there is a 13 kb deletion of sequence present in wild-type DNA and presence of a 7 kb fragment that is not present in wild-type DNA (J:10750).
  • mutations:
  • Deletion
  • synonyms:
  • steel 12 Harwell,
  • steel 12 Harwell,
  • SCF,
  • Kitl<Sl-12H>,
  • Del(10)Sl<12>1H,
  • Del(10)Sl<12>1H,
  • SCF,
  • Kitl<Sl-12H>
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1 Feature

Trail: Allele

Genome

0 Expresses

1 Mutation Involves

Trail: Allele

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

6 Publication categories

Trail: Allele