Gene: SCNN1G ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 Biomarker disease GENOMICS_ENGLAND Pseudohypoaldosteronism type 1 and Liddle's syndrome mutations that affect the single-channel properties of the epithelial Na+ channel. 26537344 2015
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 GermlineCausalMutation disease ORPHANET Clinical and molecular features of type 1 pseudohypoaldosteronism. 19571553 2009
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 Biomarker disease GENOMICS_ENGLAND A novel epithelial sodium channel gamma-subunit de novo frameshift mutation leads to Liddle syndrome. 17634077 2007
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 GermlineCausalMutation disease ORPHANET Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G-->A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1. 11231969 2001
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 Biomarker disease CTD_human A novel splice-site mutation in the gamma subunit of the epithelial sodium channel gene in three pseudohypoaldosteronism type 1 families. 8640238 1996
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G 		0.700 CausalMutation disease CLINVAR