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Hoxa13Hd
Spontaneous Allele Detail
Nomenclature
Symbol: Hoxa13Hd
Name: homeobox A13; hypodactyly
MGI ID: MGI:1857336
Synonyms: Hd
Gene: Hoxa13  Location: Chr6:52257694-52260803 bp, - strand  Genetic Position: Chr6, 25.41 cM
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
Inheritance:    Semidominant
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 7 assay results
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:  1 strain or line 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/19/2014
MGI 5.19
The Jackson Laboratory