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Human Disease and Mouse Model Detail
Human Disease Chromosome 16p11.2 Deletion Syndrome, 593-Kb
OMIM ID: 611913
Synonyms Autism; Chromosome Deletion Syndrome
View all models View ALL (1) mouse models for this human disease.
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.
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(7Coro1a-Spn)1Dolm View 1 model
References Disease References using Mouse Models (1)

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
12/09/2014
MGI 5.20
The Jackson Laboratory