About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease 3mc Syndrome 1; 3MC1
OMIM ID: 257920
Synonyms Craniosynostosis with Lid Anomalies; Michels Syndrome, Formerly; Oculopalatoskeletal Syndrome
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
     MASP1*   0:1 Homology
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
06/05/2013
MGI 5.13 		The Jackson Laboratory