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This phenotypic mutant was identified in an ENU mutagenesis screen at The Oak Ridge National Laboratory. No mutation was found in coding sequences of this gene, suggesting that the mutation is in an unidentified exon or in regulatory elements, or that sequencing the heterozygous DNA did not reveal the responsible lesion. (J:96673)
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
