About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Adams-Oliver Syndrome 1; AOS1
OMIM ID: 100300
Human Phenotype Ontology associations
Synonyms Absence Defect of Limbs, Scalp, and Skull; Adams Oliver Syndrome; Aos; Congenital Scalp Defects with Distal Limb Reduction Anomalies
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
     ARHGAP31* Arhgap31   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory