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EN
This mutation was discovered in a gene-specific sequence screen of G1 progeny of an ENU-mutagenized male mouse. It comprises an A to G transition at position 898 of the transcript (GenBank Accession 156849) that is predicted to result in replacement of aspartic acid by glycine at amino acid position 240 of the receptor protein (D240G), in the sixth leucine-rich repeat. (J:156849)
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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References Literature
Title
PMID
Journal
Year
IF
