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Complementation testing demonstrated that this mutation is an allele of the original brown (Tyrp1b) mutation. The Tyrp1b-c allele was found among (DBA/1 X C57BL/10)F1 offspring. Because DBA is homozygous for Tyrp1b, the mutation occurred on C57BL10.
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
