abnormal periodontal ligament morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the fibrous connective tissue that surrounds the root of a tooth, separating it from and attaching it to the alveolar bone; normally extends from the base of the gingival mucosa to the fundus of the bony socket, and its main function is to hold the tooth in its socket (Mammalian Phenotype Ontology, MP_0003668)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003668
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5 gene mutations causing the abnormal periodontal ligament morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANTXR1 anthrax toxin receptor 1
CTSV cathepsin V
DCN decorin
ITGA11 integrin, alpha 11
POSTN periostin, osteoblast specific factor