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Human Disease and Mouse Model Detail
Human Disease Netherton Syndrome; NETH
OMIM ID: 256500
Human Phenotype Ontology associations
Synonyms Comel-Netherton Syndrome; Erythroderma, Ichthyosiform, with Hypotrichosis and Hyper-Ige; Netherton Disease; NS
View all models View ALL (8) 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
     SPINK5* Spink5* View 5 models HomoloGene and HGNC
     DSG4 Dsg4* View 2 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(IVL-KLK5)#Hov View 1 model
References Disease References using Mouse Models (9)

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