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The Myh6 promoter was used to drive cardiac-specific expression of an Tnnt2 cDNA containing nucleotide deletions that lead to the exclusion of lysine at position 210. This mutation mimics one found in patients with dilated cardiomyopathy. Four lines were generated with similar phenotype. No line numbers were given. (J:137964)
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：
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References Literature
Title
PMID
Journal
Year
IF
