About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease

Term: Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
OMIM ID: 605594

Synonyms DFNA39/Dentinogenesis Imperfecta 1 Syndrome; DFNA39/DGI1 Syndrome; DGI1/DFNA39 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...
     
Dspp DSPP
  human...the human gene.
     MGI data currently do not associate this disease with mutations in the orthologous mouse gene.
     
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