About   Help   FAQ
Tyrc-Bc2
Spontaneous Allele Detail
Summary
Symbol: Tyrc-Bc2
Name: tyrosinase; albino 2 British Columbia
MGI ID: MGI:1856302
Synonyms: c2Bc
Gene: Tyr  Location: Chr7:87073979-87142637 bp, - strand  Genetic Position: Chr7, 49.01 cM
Alliance: Tyrc-Bc2 page
Mutation
origin
Strain of Origin:  SELH/Bc
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThis mutation comprises a deletion of exons 1, 2, and 3 of the Tyr gene but the neighboring lethality locus is not involved. (J:18053)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Tyr Mutation:  379 strains or lines available
References
Original:  J:18053 Juriloff DM, et al., Three spontaneous mutations at the albino locus in SELH/Bc mice. Genome. 1994 Apr;37(2):190-7
All:  1 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory