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Wdr19dmhd
Chemically induced Allele Detail
Summary
Symbol: Wdr19dmhd
Name: WD repeat domain 19; diamondhead
MGI ID: MGI:5315748
Synonyms: Ift144dmhd
Gene: Wdr19  Location: Chr5:65357039-65417758 bp, + strand  Genetic Position: Chr5, 33.58 cM
Alliance: Wdr19dmhd page
Mutation
origin
Strain of Origin:  FVB/NJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsENU induced a splice site mutation predicted to truncate the protein in a site prior to the TPR domains. (J:181888)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 32 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Wdr19 Mutation:  32 strains or lines available
References
Original:  J:181888 Ashe A, et al., Mutations in mouse Ift144 model the craniofacial, limb and rib defects in skeletal ciliopathies. Hum Mol Genet. 2012 Apr 15;21(8):1808-23
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory