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Human Disease and Mouse Model Detail
Human Disease Split-Hand/Foot Malformation 1; SHFM1
OMIM ID: 183600
Human Phenotype Ontology associations
Synonyms Ectrodactyly; ECD; Split-Hand Deformity; Split-Hand/Foot Deformity 1; SHFD1; SHSF1; Split-Hand/Foot Malformation; Split-Hand/Foot Malformation 1 with or without Deafness
View all models View ALL (3) 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
     DLX5 Dlx5* View 1 model HomoloGene and HGNC
DLX6 Dlx6* View 1 model 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(6Dlx6-Dlx5)1Tlu View 1 model
References Disease References using Mouse Models (2)

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