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

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

Strain of Origin:

C57BL/6

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

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

In Structures Affected by this Mutation:

3 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:13417 Hollander WF, mi. Mouse News Lett. 1964;30:29
All:	8 reference(s)