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Foxn1nu
Spontaneous Allele Detail
Summary
Symbol: Foxn1nu
Name: forkhead box N1; nude
MGI ID: MGI:1856108
Synonyms: Foxnlnu, hairless, nu, Whn-
Gene: Foxn1  Location: Chr11:78248403-78277384 bp, - strand  Genetic Position: Chr11, 46.74 cM
Alliance: Foxn1nu page
Control and Foxn1nu/Foxn1nu

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  albino stock
Mutation
description
Allele Type:    Spontaneous (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsA single base pair (G) deletion in exon 3 introduces a frameshift and a premature stop codon. The encoded protein is predicted to terminate upstream of the DNA-binding domain. (J:21194)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 121 assay results
2 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 36 anatomical structure(s)
Tumor Data
List all tumor models in MMHCdb carrying Foxn1nu
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 43 strains available      Cell Lines: 0 lines available
Carrying any Foxn1 Mutation:  96 strains or lines available
References
Original:  J:30772 Isaacson JH, et al., Two new 'hairless' mutants - Sha and Hfh11. Mouse News Lett. 1962;27:31
All:  451 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
02/20/2024
MGI 6.23
The Jackson Laboratory