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The coding region was replaced with a cDNA of the mouse gene containing a C213G mutation in exon 5 and a floxed neo cassette in inverse orientation via homologous recombination. This mutation disrupts the extracellular allosteric disulfide bond (Cys190-Cys213). (J:309113)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
