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MitfMi-H
Chemically induced Allele Detail
Nomenclature
Symbol: MitfMi-H
Name: melanogenesis associated transcription factor; microphthalmia Harwell
MGI ID: MGI:2178353
Synonyms: Gena163, GENA 163
Gene: Mitf  Location: Chr6:97807052-98021349 bp, + strand  Genetic Position: Chr6, 45.05 cM
Mutation
origin
Strain of Origin:  (C3H/HeN x BALB/cAnN)F1
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Undefined
    The mutation underlying the phenotype in Mi-H mice was reported as a splicing defect. (J:75964)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 8 anatomical structures
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:  60 strains or lines available
References
Original:  J:75964 Thaung C, et al., Novel ENU-induced eye mutations in the mouse: models for human eye disease. Hum Mol Genet. 2002 Apr 1;11(7):755-67
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/15/2018
MGI 6.12
The Jackson Laboratory