DisGeNET - a database of gene-disease associations

Source: MGD

Disease: Heterotaxy, Visceral, 3, Autosomal ×

Gene: AP1B1 ×

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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

Gene Full Name

DSI _g

DPI _g

pLI

Disease

Type

Score _gda

EL_gda

EI _gda

N.PMIDs

N.SNPs _gda

First Ref.

LastRef.

Entrez Id:	162
Gene Symbol:	AP1B1

AP1B1

adaptor related protein complex 1 subunit beta 1

0.716

0.385

1.00

CUI:	C1853444
Disease:	Heterotaxy, Visceral, 3, Autosomal

Heterotaxy, Visceral, 3, Autosomal

disease

0.200

None

0