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Hoxd13Dyc
Spontaneous Allele Detail
Summary
Symbol: Hoxd13Dyc
Name: homeobox D13; digit in Y-shaped finger and carpe
MGI ID: MGI:4361275
Gene: Hoxd13  Location: Chr2:74498654-74501943 bp, + strand  Genetic Position: Chr2, 44.13 cM
Alliance: Hoxd13Dyc page
Mutation
origin
Strain of Origin:  BALB/c
Mutation
description
Allele Type:    Spontaneous
Mutations:    Duplication, Nucleotide repeat expansion
 
Mutation detailsSpontaneous duplications, likely due to fork stalling and template switching, expand the polyalanine stretch in exon 1 from 15 to 22 alanines. (J:153164)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 8 assay results
In Structures Affected by this Mutation: 10 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 Hoxd13 Mutation:  24 strains or lines available
References
Original:  J:153164 Cocquempot O, et al., Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactyly. Genetics. 2009 Sep;183(1):23-30
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