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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
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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)
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last database update
10/22/2024
MGI 6.24
The Jackson Laboratory