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A mouse Tyro3 cDNA sequence with a C19T point mutation, which results in an arginine to tryptophan substitution at the 7th amino acid to mimic the point mutation in Tyro3m1, and a c-terminal GFP sequence was randomly inserted into the genome. (J:241666)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
