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Human Disease and Mouse Model Detail
Human Disease Velocardiofacial Syndrome
OMIM ID: 192430
Synonyms Chromosome 22q11.2 Deletion Syndrome; Shprintzen Vcf Syndrome; VCF Syndrome; VCFS
View all models View ALL (11) 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
     Tbx1* TBX1* View 5 models 1:1 Homology
     b2b1941Clo* View 1 model
Chrd* CHRD View 1 model 1:1 Homology
Crkl* CRKL View 1 model 1:1 Homology
Ednra* EDNRA View 1 model 1:1 Homology
Prickle1* PRICKLE1 View 1 model 1:1 Homology
     Dgcr2 DGCR2*   1:1 Homology
DGCR6*, LOC102724770   0:2 Homology
Dgcr8 DGCR8*   1:1 Homology
Dgcr14 DGCR14*   1:1 Homology
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(16Dgcr2-Hira)1Rak View 1 model
References Disease References using Mouse Models (8)

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 5.20
The Jackson Laboratory