DisGeNET - a database of gene-disease associations

Retinal Dystrophies, C0854723

Gene: DRAM2 ×

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:	128338
Gene Symbol:	DRAM2

DRAM2

0.110

GeneticVariation

group

BEFREE

To determine the disease course of retinal dystrophy caused by recessive variants in the DRAM2 (damage-regulated autophagy modulator 2) gene.

2015

Entrez Id:	128338
Gene Symbol:	DRAM2

DRAM2

0.110

CausalMutation

group

CLINVAR

Entrez Id:	128338
Gene Symbol:	DRAM2

DRAM2

0.110

Biomarker

group

HPO