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Human Disease and Mouse Model Detail
Human Disease Wolf-Hirschhorn Syndrome; WHS
OMIM ID: 194190
Human Phenotype Ontology associations
Synonyms Chromosome 4p16.3 Deletion Syndrome; Pitt Syndrome; Pitt-Rogers-Danks Syndrome; PRDS; Wittwer Syndrome
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     FGFRL1* Fgfrl1* View 1 model HomoloGene and HGNC
NSD2* Nsd2* View 2 models HomoloGene and HGNC
     CPLX1* Cplx1   HomoloGene and HGNC
CTBP1* Ctbp1   HomoloGene and HGNC
LETM1* Letm1   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
  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
References Disease References using Mouse Models (3)

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