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Allele : Hoxd13<spdh> homeobox D13; synpolydactyly homolog

Primary Identifier  MGI:1857397 Allele Type  Spontaneous
Gene  Hoxd13 Inheritance Mode  Recessive
Strain of Origin  B6C3Fe a/a-Csf1<op>/J Is Recombinase  false
Is Wild Type  false
molecularNote  21 bp in-frame duplication within a polyalanine-encoding region at the 5'-end of the Hoxd13 coding sequence. This duplication expands the stretch of alanines from 15 to 22, the same type of expansion that occurs in human synpolydactyly mutations.
  • mutations:
  • Insertion
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

Trail: Allele

0 Driven By

9 Publication categories

Trail: Allele