Mitf^mi-x39
Radiation induced Allele Detail

Summary

• Symbol: Mitf^mi-x39
• Name: melanogenesis associated transcription factor; microphthalmia x39
• MGI ID: MGI:2148647
• Gene: Mitf Location: Chr6:97784013-97998310 bp, + strand Genetic Position: Chr6, 45.05 cM
• Alliance: Mitf^mi-x39 page

Mutation origin

• Strain of Origin: (102 x C3H)F1

Mutation description

• Allele Type: Radiation induced
• Mutation: Intragenic deletion
• Mutation details: A 1408 bp deletion starting 705 bp upstream of exon 4 and ending 607 bp downstream of exon 4. This mutation also affects exon 3 splicing, and results in exon 3 skipping in some cases. (J:62098)
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

3 anatomical structure(s)

Find Mice (IMSR)

• 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 Mitf Mutation: 74 strains or lines available

References

• Original: J:62098 Hallsson JH, et al., Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus. Genetics. 2000 May;155(1):291-300
• All: 1 reference(s)