DisGeNET - a database of gene-disease associations

Asthenozoospermia, C0403823

Gene: HNF1B ×

Source: ALL

Results per page

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

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	6928
Gene Symbol:	HNF1B

HNF1B

0.110

GeneticVariation

disease

BEFREE

Structural malformation of male urogenital tract is rare in MODY 5, even rarer is asthenospermia.

2018

Entrez Id:	6928
Gene Symbol:	HNF1B

HNF1B

0.110

Biomarker

disease

HPO