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The transgenic construct encodes a deletion in fat-specific element(FSE)region of human GPD1 promoter (deletes from -258 to -135, or 124 bp). A second strain, d124B, was also created (2-5 copies in each) and two shorter deletion (36 bp) mutants (d36A, d36B) were generated. (J:135002)
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 |
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References Literature
Title
PMID
Journal
Year
IF
