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Hoxa13Hd
Spontaneous Allele Detail
Summary
Symbol: Hoxa13Hd
Name: homeobox A13; hypodactyly
MGI ID: MGI:1857336
Synonyms: Hd
Gene: Hoxa13  Location: Chr6:52235833-52237865 bp, - strand  Genetic Position: Chr6, 25.41 cM
Alliance: Hoxa13Hd page
Hoxa13Hd/+ and control

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  MYA/Hu
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation details: A 50-base pair deletion in the first exon of the Hd allele that probably arose from unequal recombination or misalignment between triplet repeats. (J:33715)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 52 assay results
In Structures Affected by this Mutation: 26 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Hoxa13 Mutation:  29 strains or lines available
Notes

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).
References
Original:  J:64253 Hummel KP, et al., Hd - hypodactyly. Mouse News Lett. 1966;34:31
All:  11 reference(s)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory