DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: Anoxia ×

Gene: KCNMB1 ×

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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:	3779
Gene Symbol:	KCNMB1

KCNMB1

CUI:	C0003130
Disease:	Anoxia

Anoxia

0.010

AlteredExpression

LHGDN

Post-transcriptional control of human maxiK potassium channel activity and acute oxygen sensitivity by chronic hypoxia.

2003