Several inbred strain (BALB/cHeA, BALB/cAnN, 129/SvJ, and C.B17) harbors an A-to-G transition at position 11530 resulting in a methonine to valine substitution at codon 3844 and a C-to-T transition at position 6418 resulting in an arginine to cysteine substitution at codon 2140. This allele is associated with decreased gene expression and protein activity and severe susceptibility to induced nephropathy. C57BL6/J, FVB/NJ and CAST/EiJ demonstrated strong resistance to DOX nephropathy. The susceptibility allele contains a C6418T transition in exon 48 that results in the amino acid substitution of cystein for arginine at position 2140 (R2140C). (J:70283, J:96632, J:166909)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
multiple strains
Spontaneous
Undefined
Recessive
1
2
6

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

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PMID
Journal
Year
IF
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