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Human Disease and Mouse Model Detail
Human Disease Wolf-Hirschhorn Syndrome; WHS
OMIM ID: 194190
Synonyms Chromosome 4p16.3 Deletion Syndrome; Pitt Syndrome; Pitt-Rogers-Danks Syndrome; PRDS
View all models View ALL (7) 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
     Whsc1* WHSC1* View 2 models 1:1 Homology
     Fgfrl1* FGFRL1 View 1 model 1:1 Homology
     WHCR*  
Transgenes and
other genome features 		Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Del(5D5Mit73-D5Mit351)5Jcs View 1 model
  Del(5D5Mit148-Qdpr)2Jcs View 1 model
  Del(5D5Mit388-D5Mit351)4Jcs View 1 model
  Del(5LetM1-D5Mit81)3Jcs View 1 model
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
06/12/2013
MGI 5.14 		The Jackson Laboratory