Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD A quantitative survey of gravity receptor function in mutant mouse strains. 16235133

2005
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD Postural and locomotor control in normal and vestibularly deficient mice. 15243133

2004
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD Altered potassium balance and aldosterone secretion in a mouse model of human congenital long QT syndrome. 11438691

2001
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD KCNQ1/KCNE1 potassium channels in mammalian vestibular dark cells. 11223304

2001
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD A new spontaneous mouse mutation in the Kcne1 gene. 11003695

2000
Entrez Id: 102723475
Gene Symbol: KCNE1B
KCNE1B
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		0.200 Biomarker MGD Inner ear defects induced by null mutation of the isk gene. 8982171

1996