pierre-robin sequence Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Pierre Robin malformation is a sequence of developmental malformations characterized by micrognathia (mandibular hypoplasia), glossoptosis and cleft palate. (Human Phenotype Ontology, HP_0000201)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000201
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7 genes associated with the pierre-robin sequence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
COL2A1 collagen, type II, alpha 1
EIF4A3 eukaryotic translation initiation factor 4A3
PGM1 phosphoglucomutase 1
TBX1 T-box 1