An isoform specific mutation was generated by replacing the coding region of exon 1B with a floxed neomycin selection cassette. RT-PCR analysis verified that sequence upstream of the insertion, encoding the A isoform, was transcribed. Transcript encoding the B isoform was undected in homozygous mutant mice by RT-PCR analysis. (J:82249)

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
6
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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