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A 5' genomic region of the human CETP including 138 base pairs of flanking sequence, exon1, intron 1 and part of exon 2 was linked using a fragment of human CETP cDNA to a 3' sequence of the same gene made up of part of exon 13, exons 14-16, introns 13-15, and 121 base pairs of flanking sequence. The resulting construct lacks introns 2-12. One male and one female founder were identified but a line was established only from the female founder. Only one copy of the transgene was inserted. (J:93800)
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
