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

Symbol:	Ift172wim
Name:	intraflagellar transport 172; wimple
MGI ID:	MGI:2682066
Synonyms:	Ift172wim
Gene:	Ift172  Location: Chr5:31410623-31448458 bp, - strand  Genetic Position: Chr5, 17.27 cM, cytoband B1
Alliance:	Ift172wim page

Strain of Origin:

C57BL/6J

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: An ENU-induced T-to-C mutation results in a leucine to proline substitution at position 1564 (p.L1564P). Inheritance:    Recessive

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

In Mice Carrying this Mutation:	31 assay results
In Structures Affected by this Mutation:	7 anatomical structure(s)

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 Ift172 Mutation:	75 strains or lines available

Original:	J:86437 Huangfu D, et al., Hedgehog signalling in the mouse requires intraflagellar transport proteins. Nature. 2003 Nov 6;426(6962):83-7
All:	15 reference(s)