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Human Disease and Mouse Model Detail
Human Disease Deafness, Autosomal Dominant 39, with Dentinogenesis Imperfecta 1
OMIM ID: 605594
Synonyms DFNA39/Dentinogenesis Imperfecta 1 Syndrome; DFNA39/DGI1 Syndrome; DGI1/DFNA39 Syndrome
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     DSPP*  

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/23/2014
MGI 5.19
The Jackson Laboratory