Jervell-Lange Nielsen Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2842)
External Link https://www.disgenet.org/browser/0/1/0/C0022387
Similar Terms
Downloads & Tools

Genes

10 genes associated with the disease Jervell-Lange Nielsen Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
GAST gastrin
HFE hemochromatosis
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
LOC102723475 putative uncharacterized protein LOC388820
NT5E 5'-nucleotidase, ecto (CD73)
SCN5A sodium channel, voltage gated, type V alpha subunit