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

Symbol: Fgf10ptls Name: fibroblast growth factor 10; pootloos MGI ID: MGI:4849925 Synonyms: Fgf10L91P Gene: Fgf10  Location: Chr13:118851199-118928651 bp, + strand  Genetic Position: Chr13, 67.14 cM, cytoband A3-A4 Alliance: Fgf10ptls page

Absence of limbs and lungs in Fgf10ptls/Fgf10ptls embryos Show the 1 phenotype image(s) involving this allele.

Strain of Origin:

C57BL/6

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: ENU-mutagenesis induced a T to C transition that results in the amino acid substitution of leucine with proline at position 91 (p.L91P). (J:173681) Inheritance:    Recessive

Identification of a leucine-to-proline substitution in the FGF domain of Fgf10ptls allele

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

In Structures Affected by this Mutation:

3 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 Fgf10 Mutation:	33 strains or lines available

Original:	J:167035 Meijlink F, et al., Hubrecht Institute ENU screen. MGI Direct Data Submission. 2011;
All:	2 reference(s)