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Allele : Hoxa13<Hd> homeobox A13; hypodactyly

Primary Identifier  MGI:1857336 Allele Type  Spontaneous
Gene  Hoxa13 Inheritance Mode  Semidominant
Strain of Origin  MYA/Hu Is Recombinase  false
Is Wild Type  false
description 

A double mutant of the hydrocephalic-polydactyly mutation, hophpy, and the hypodactyly mutation, Hoxa13Hd, produced offspring of normal hallux phenotype. The first mutant tends to multiply, the second to eliminate halluces, and the two cancel each other (J:23839).

molecularNote  A 50-base pair deletion in the first exon of the Hd allele that probably arose from unequal recombination or misalignment between triplet repeats.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Hd,
  • Hd
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

13 Carried By

Trail: Allele

0 Driven By

12 Publication categories

Trail: Allele