About   Help   FAQ
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
Loading...
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory