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Human Disease and Mouse Model Detail
Human Disease Spondyloepiphyseal Dysplasia Congenita; SEDC
OMIM ID: 183900
Synonyms SED Congenita; Spondyloepiphyseal Dysplasia, Congenital Type
View all models View ALL (6) mouse models for this human disease.
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
     Col2a1* COL2A1* View 4 models 1:1 Homology
     Hapln1* HAPLN1 View 1 model 1:1 Homology
Transgenes and
other genome features 		Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Col2a1*R789C)#Waho View 1 model
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
06/05/2013
MGI 5.13 		The Jackson Laboratory