Sequence encompassing the entire open reading frame, which is contained in the 5' region of exon 2, was flanked by an upstream loxP site in intron 1 and a downstream floxed neo cassette. The entire open reading frame and the neo transgene were excised via cre recombinase mediated deletion. Northern blot analysis and in situ hybridization showed an absence of transcript in homozygous mutant mice. A complete absence of encoded protein was determined via Western blot analysis using antibodies for the amino and carboxy termini. (J:71372)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Targeted
Intragenic deletion
--
1
--
31

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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