Transient Cre expression in embryonic stem cells whose endogenous gene bore previous modifications, including loxP sites flanking a 2000-base pair segment, resulted in deletion of exons 5 through 11, which encode most of the region common to all three receptor isoforms; this mutant allele also contains a previously introduced frt-flanked Pgk-neomycin phosphotransferase cassette in intron 11 and a deletion of 3.9 kb from intron 4. (J:93288)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Targeted
Insertion, Intragenic deletion
--
1
3
1

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

References Literature

Title
PMID
Journal
Year
IF
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