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Hdlk
Spontaneous Allele Detail
Summary
Symbol: Hdlk
Name: hypodactyly like
MGI ID: MGI:4367718
Gene: Hdlk  Location: Chr6:50841914-55533028 bp  Genetic Position: Chr6, Syntenic
Alliance: Hdlk page
Oligodactyly in Hdlk/Hdlk mice

Show the 2 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    This spontaneous mutation was identified at The Jackson Laboratory.
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 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 Hdlk Mutation:  1 strain or line available
References
Original:  J:154358 Karst SY, et al., Hypodactyly like: a mutation causing fused and missing digits is likely an allele of the Hoxa13 gene. MGI Direct Data Submission. 2009;
All:  1 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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory