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

Symbol:	Tyrc-26DVT
Name:	tyrosinase; albino deletion 26DVT, Oak Ridge
MGI ID:	MGI:2153742
Synonyms:	c26DVT, cFp1, Df(c Mod-2 sh-1)26DVT, Tyrc-49R, Tyrc-Fp1
Gene:	Tyr  Location: Chr7:87073979-87142637 bp, - strand  Genetic Position: Chr7, 49.01 cM
Alliance:	Tyrc-26DVT page

Strain of Origin:

(101/Rl x C3H/Rl)F1

Allele Type:    Radiation induced Mutation:    Deletion   Tyrc-26DVT involves 139 genes/genome features (Fah, Zfand6, 2610206C17Rik ...) View all   Mutation details: This multi-locus deletion, induced by X-ray irradiation of a male mouse, encompasses G-bands 7D3-7E3 and includes, proximally, Fah (fumarylacetoacetate hydrolase) and distally, Aqp11 (aquaporin 11; formerly sjds). The deletion is flanked proximally by Mesdc2, mesoderm development candidate 2, and distally by Hbb, the hemoglobin beta chain complex. (J:54592, J:100221) Inheritance:    Recessive

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

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Tyr Mutation:	375 strains or lines available

Original:	J:23420 Russell LB, et al., Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies. Genetics. 1982 Mar;100(3):427-53
All:	13 reference(s)