Part of exon and intron 2 were replaced with a neo cassette. The absence of transcript was confirmed by whole mount in situ hybridization using E8.5 embryos. An aberrant transcript lacking the 471 N-terminal amino acids is produced from an initiation site in exon 3. The lack of the full-length protein product and presence of a shorter peptide lacking the N-terminus was confirmed by western blot analysis on embryonic fibroblasts derived from E8.5 embryos. (J:127131)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(129X1/SvJ x 129S1/Sv)F1-Kitl+
Targeted
Insertion, Intragenic deletion
--
1
--
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:
Show/Hide columns
Phenotypes

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
Wechat
Comparison
Al agent
Tutorials
Back to top