Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

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

Strain of Origin:

FVB/NJ

Allele Type:    Chemically induced (ENU) Mutation:    Nucleotide substitutions   Mutation details: ENU induced a splice site mutation predicted to truncate the protein in a site prior to the TPR domains. (J:181888) Inheritance:    Recessive

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:

32 assay results

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

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)