This chromosomal aberration comprises a deletion of at least 1 cM in length that affects these loci: Tyr, jdf, Mod2, Eed, and exed. (J:2961, J:5437)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
(C3H/HeH x 101/H)F1
Radiation induced
Intergenic deletion
Recessive
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--
12

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
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