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A transgene derived from a human bacterial artificial chromosome (BAC) library, containing the entire human UGT1 (UDP glucuronosyltransferase 1) complex, was modified by targeted mutation of the UGT1 polypeptide A1, UGT1A1, promoter to harbor the UGT1A1*28 mutation associated with hepatic dysfunction found in Gilbert's syndrome. Specifically, this mutation inserts an extra TA in the TATA box sequence of the UGTA1A promoter. Five founders were generated. Founder mice from line 1 carry 6 copies of the transgene on Chromosome 15. (J:102898)
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
