CRISPR/Cas9 technology generated a G to A change resulting in an arginine to glutamine substitution at amino acid 400 (p.R400Q) in exon 13. This is a rare mutation seen in individuals with cardiomyopathy. (J:342938)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(C57BL/6J x CBA)F2
Endonuclease-mediated
Single point
--
1
15
1

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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