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Human Disease and Mouse Model Detail
Human Disease Stargardt Disease 3; STGD3
OMIM ID: 600110
Human Phenotype Ontology associations
Synonyms Macular Dystrophy with Flecks, Type 3; Stargardt Disease; Stargardt-Like Macular Dystrophy, Autosomal Dominant
View all models View ALL (5) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ELOVL4 Elovl4* View 5 models HomoloGene and HGNC
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(RBP3-ELOVL4*)1Kzh View 1 model
  Tg(RBP3-ELOVL4*)2Kzh View 1 model
  Tg(RBP3-ELOVL4*)3Kzh View 1 model
References Disease References using Mouse Models (6)

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
MGI 6.07
The Jackson Laboratory