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Allele : T(16;17)43H reciprocal translocation, Chr 16 and 17, Harwell 43
Primary Identifier  MGI:3574967 Allele Type  Radiation induced
Gene  T(16;17)43H Strain of Origin  (C3H/HeH x 101/H)F1
Is Recombinase  false Is Wild Type  false
molecularNote  This chromosome is a result of a reciprocal translocation with one breakpoint located within the centromeric heterochromatin of Chr16, and the other located in the B3 band of Chr17. In conjunction with a normal Chr16 and two normal Chr17s, the presence of this mutation results in segmental trisomy of the proximal 30 Mb of Chr17, which includes over 310 known genes, and monosomy for the tip of centromeric heterochromatin of Chr16.
  • mutations:
  • Translocation
  • synonyms:
  • T43,
  • Ts43H,
  • Ts43H,
  • T43
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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2 Carried By

Trail: Allele

0 Driven By

7 Publication categories

Trail: Allele




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