An Nfkbia cDNA fragment encoding amino acids 71 through 317 of Nfkbia was inserted at start codon of the endogenous gene. The coding region of the first coding exon and the following 4 downstream exons were replaced by the inserted sequences. The encoded mutant Nfkbia protein was expressed in most tissues, lacked the N-terminal destruction box degradation signal, and has been previously shown to inhibit Nfkb1. (J:71744)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129P2/OlaHsd
Targeted
Insertion, Intragenic deletion
--
1
22
8

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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