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This deletion was created by cre mediated recombination in ES cells of loxP sites within targeted knock-ins at Abcg1 (containing a duplicated exons 14 and 15, neo cassette, loxP site, and 5' Hprt minigene; Abcg1tm1Yah) and between Cba and U2af1 (containing a 3' Hprt mini gene, loxP, and puro cassette; Is(17B1)1Yah). The deletion spans a 0.59 Mb interval between Abcg1 and U2af1 that contains part of Abcg1, all of Tff3, Tff2, Tff1, Tmprss3, Ubash3a, Rsph1, Slc37a1, Pde9a, Wdr4, 1500032D16RIK (Ndufv3), Pknox1, and Cbs but does not include U2af1. (J:154298)
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
