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Human Disease and Mouse Model Detail
Human Disease

Term: Hand-Foot-Uterus Syndrome
OMIM ID: 140000

Synonyms Hand-Foot-Genital Syndrome; HFG Syndrome; HFU Syndrome
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...
Hoxa13 HOXA13
  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
Hoxa13Hd/Hoxa13Hd   involves: MYA/Hu J:5211, J:64253
Hoxa13Hd/Hoxa13Hd   B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J J:58731
Hoxa13Hd/Hoxa13+   B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J J:54823
Hoxa13tm1Jwi/Hoxa13tm1Jwi   involves: 129S7/SvEvBrd J:94412
Hoxa13tm1Jwi/Hoxa13+   involves: 129S7/SvEvBrd J:94412

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
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory