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

Symbol:	Mitfmi-di
Name:	melanogenesis associated transcription factor; microphthalmia defective iris
MGI ID:	MGI:1856090
Gene:	Mitf  Location: Chr6:97784013-97998310 bp, + strand  Genetic Position: Chr6, 45.05 cM
Alliance:	Mitfmi-di page

Strain of Origin:

(PT x C3H/HeH)F1

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation     C to T transition at bp 916 that introduces a stop codon after amino acid 262. (J:62098) Inheritance:    Recessive

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

In Mice Carrying this Mutation:	2 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: 1 strain available      Cell Lines: 0 lines available
Carrying any Mitf Mutation:	72 strains or lines available

Original:	J:65315 West JD, et al., Mitfmi-di - microphthalmia-defective iris. Mouse News Lett. 1985;72:106
All:	3 reference(s)