Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Tumor data | Find Mice (IMSR) | References

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.

Strain of Origin:

albino stock

Allele Type:    Spontaneous (Null/knockout) Mutation:    Intragenic deletion   Mutation details: A 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

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	121 assay results 3 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	34 anatomical structure(s)

List all tumor models in MMHCdb carrying Foxn1nu

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:	106 strains or lines available

Original:	J:30772 Isaacson JH, et al., Two new 'hairless' mutants - Sha and Hfh11. Mouse News Lett. 1962;27:31
All:	498 reference(s)