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EN
A hypomorphic allele was generated by the insertion of a full length myogenin cDNA followed by an SV40 T polyadenylation site and a loxP-flanked neomycin cassette into the first exon and deletion of basepairs +48 to +511. Transcript was present at approximately one-fourth the level of controls in muscle. The mutant genomic sequence still contains the transcription start site and the splice donor of the first exon. (J:54065)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
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 |
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References Literature
Title
PMID
Journal
Year
IF
