About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: T-Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
OMIM ID: 601705

Associated Genes

Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.

Mouse Gene
Human Gene
 
Characteristics of this human disease are associated with mutations in...
Foxn1 FOXN1
  mousehuman...both mouse and human orthologous genes.
     

Mouse Models
Genotype Ref(s)
Allelic Composition Note Genetic Background
Models with phenotypic similarity to human disease where etiologies involve orthologs.1
Foxn1nu-Y/Foxn1nu-Y   101/HY-Foxn1nu-Y J:29022
Foxn1nu/Foxn1nu   Not Specified J:11959
Foxn1tm1Tbo/Foxn1tm1Tbo   involves: 129S1/Sv J:33796

1Human genes are associated with this disease. Mouse model genotypes include mutations in the orthologs of these human genes.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory