This is a 595,992bp deletion on Chromosome 1. Using Build 37 (mm9), the centromeric break point is at 75,098,488 bp and the telomeric breakpoint is at 75,694,480 bp. (J:135300)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
(C3H/HeH x 101/H)F1
Spontaneous
Intergenic deletion
Dominant
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8

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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