Gene: POMT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 29954
Gene Symbol: POMT2
POMT2 		0.110 GeneticVariation disease BEFREE Our results broaden the clinical spectrum associated with POMT2 mutations, which should be considered in patients with CMD associated with microcephaly, and severe mental retardation with or without ocular involvement. 17634419 2007
Entrez Id: 29954
Gene Symbol: POMT2
POMT2 		0.110 Biomarker disease HPO