Mitf<Mi-ws> Radiation induced Allele Detail MGI Mouse (MGI:1856093)

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

Phenotypes

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

Expression

In Structures Affected by this Mutation:

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)

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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