Gene: SCLT1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.320 GeneticVariation disease BEFREE Sodium channel and clathrin linker 1 (SCLT1) mutations were associated with the oral-facial-digital syndrome (OFD), an autosomal recessive ciliopathy. 28486600 2017
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.320 Biomarker disease GENOMICS_ENGLAND Ciliary genes TBC1D32/C6orf170 and SCLT1 are mutated in patients with OFD type IX. 24285566 2014
Entrez Id: 132320
Gene Symbol: SCLT1
SCLT1 		0.320 GeneticVariation disease BEFREE The molecular composition of DAPs was recently elucidated and mutations in two genes encoding DAPs components (CEP164/NPHP15, SCLT1) have been associated with human ciliopathies, namely nephronophthisis and orofaciodigital syndrome. 24882706 2014