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The human ventricular essential light chain cDNA with an alanine to glycine mutation at residue 57 (A57G) is under the control of the mouse alpha-myosin heavy chain promoter. Lines L1, L5, and L2 were generated, however the pound symbol (#) is used when line is not specified and/or lines are pooled. (J:178377)
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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| Phenotypes |
|---|
References Literature
Title
PMID
Journal
Year
IF
