Mitf^Mi-ws
Radiation induced Allele Detail

Summary

• Symbol: Mitf^Mi-ws
• Name: melanogenesis associated transcription factor; white spot
• MGI ID: MGI:1856093
• Synonyms: mi^ws
• Gene: Mitf Location: Chr6:97784013-97998310 bp, + strand Genetic Position: Chr6, 45.05 cM
• Alliance: Mitf^Mi-ws page

Mutation origin

• Strain of Origin: C57BL/6

Mutation description

• Allele Type: Radiation induced
• Mutation: Intragenic deletion
• Mutation details: The molecular lesion is a deletion within the N-terminal region of the gene. A 4280 bp genomic deletion starts in an intron 170 bp upstream of the exon 2 splice acceptor site and ends 767 bp downstream of the exon 4 splice donor site. (J:21366, 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: 1 strain available Cell Lines: 0 lines available
• Carrying any Mitf Mutation: 74 strains or lines available

References

• Original: J:13417 Hollander WF, mi. Mouse News Lett. 1964;30:29
• All: 8 reference(s)