This allele comprises a two base pair insertion (GC) in exon 7 causing a frameshift at amino acid 372, adding 134 unique amino acids. The result is a truncated form of the transcription factor protein that retains the DNA binding domain but lacks the activation domain. This mutation is shown to be allelic to Foxn1 by lack of complementation. Uunlike the original nude allele, the protein of this allele is detected in the nucleus. (J:63313)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6
Spontaneous
Insertion
Recessive
1
4
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