Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease BEFREE Mutations in POMT1 have been identified in Walker-Warburg syndrome and in patients with limb-girdle muscular dystrophy and mental retardation (LGMD2K). 16717220 2006
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies. 22323514 2012
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation. 16575835 2006
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. 12369018 2002
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies. 17869517 2008
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. 22549409 2012
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome. 15637732 2005
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East. 18752264 2008
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardation. 16575835 2006
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome. 15637732 2005
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR POMGnT1, POMT1, and POMT2 mutations in congenital muscular dystrophies. 20816175 2010
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. 17878207 2007
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations. 24491487 2014
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Molecular heterogeneity in fetal forms of type II lissencephaly. 17559086 2007
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR A Successful Treatment of Endoscopic Third Ventriculostomy with Choroid Plexus Cauterization for Hydrocephalus in Walker-Warburg Syndrome. 28116189 2016
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome. 12369018 2002
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 CausalMutation disease CLINVAR Detection limit of intragenic deletions with targeted array comparative genomic hybridization. 24304607 2013
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR A novel missense mutation in POMT1 modulates the severe congenital muscular dystrophy phenotype associated with POMT1 nonsense mutations. 24491487 2014
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 GeneticVariation disease CLINVAR Expanding the clinical spectrum of POMT1 phenotype. 16717220 2006
Entrez Id: 10585
Gene Symbol: POMT1
POMT1 		0.710 Biomarker disease CTD_human
Entrez Id: 148789
Gene Symbol: B3GALNT2
B3GALNT2 		0.300 Biomarker disease CTD_human
Entrez Id: 84197
Gene Symbol: POMK
POMK 		0.300 Biomarker disease CTD_human
Entrez Id: 2218
Gene Symbol: FKTN
FKTN 		0.300 Biomarker disease CTD_human
Entrez Id: 79147
Gene Symbol: FKRP
FKRP 		0.300 Biomarker disease CTD_human
Entrez Id: 10329
Gene Symbol: RXYLT1
RXYLT1 		0.300 Biomarker disease CTD_human