DisGeNET - a database of gene-disease associations

INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2, C3809468

Source: ALL

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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

UniProt

Gene Full Name

Protein Class

N. diseases_g

DSI _g

DPI _g

pLI

Score _gda

EL _gda

EI _gda

N. PMIDs

N. SNPs _gda

First Ref.

Last Ref.

Entrez Id:	3181
Gene Symbol:	HNRNPA2B1

HNRNPA2B1

P22626

heterogeneous nuclear ribonucleoprotein A2/B1

131

0.566

0.808

1.00

0.400

None

1.000

1

1

2013

2013

Entrez Id:	3502
Gene Symbol:	IGHG3

IGHG3

P01860

immunoglobulin heavy constant gamma 3 (G3m marker)

161

0.513

0.769

0.010

None

1.000

1

0

2000

2000