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Mitfmi-di
Chemically induced Allele Detail
Summary
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
Mutation
origin
Strain of Origin:  (PT x C3H/HeH)F1
Mutation
description
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
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 2 assay results
In Structures Affected by this Mutation: 7 anatomical structure(s)
Find Mice (IMSR)
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:  74 strains or lines available
References
Original:  J:65315 West JD, et al., Mitfmi-di - microphthalmia-defective iris. Mouse News Lett. 1985;72:106
All:  3 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
11/12/2024
MGI 6.24
The Jackson Laboratory