Log In|Sign Up
EN
This deletion, induced by X-irradiation of a (C3H/HeH x101/H)F1 female mouse, encompasses 12.66 Mb representing approximately 20% of mouse Chr 13 including bands A3.1 through A4. The deleted segment shares synteny with regions of human 6p25 and 6p22 associated with 6p deletion syndromes and 6p associated disorders. (J:94183, 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：
Show/Hide columns
| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
