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This phenotypic mutation was identified in an ENU mutagenesis screen focused on the Del(13)39H deletion interval, which encompasses ~20% of mouse Chr 13 that shares two regions of conserved synteny with human Chr 6p22.1-6p22.3/6p25. (J:101156)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
