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A mutant human cDNA coding for the transmembrane and cytoplasmic domains of the receptor was inserted in-frame into mouse genomic sequences. The mutations resulted in alteration of a multifunctional tyrosinase motif from Y1349VHVNATY1356VNV to Y1349VNVNATY1356VNV. A floxed neo included in the construct was excised by crossing with Cre deleter mice. (J:94030)
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
