DisGeNET - a database of gene-disease associations

Gene: KCNJ18 ×

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	100134444
Gene Symbol:	KCNJ18

KCNJ18

CUI:	C3714580
Disease:	Hypokalemic periodic paralysis type 1

Hypokalemic periodic paralysis type 1

0.310

Biomarker

GENOMICS_ENGLAND

Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.

2010