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EN
The deletion is within chr 1;122,441,093-122,831,023 (mm9) telomeric to En1 was deleted to mimic the 27 kb deletion 200 kb centormeric to En1 (chr2:118,504,360-118,897,678; hg38) found in a patient with severe congenital limb malformation. (J:306235)
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
