DisGeNET - a database of gene-disease associations

Source: LHGDN

Disease: leukemia ×

Gene: RARA ×

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

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	5914
Gene Symbol:	RARA

RARA

CUI:	C0023418
Disease:	leukemia

leukemia

0.100

GeneticVariation

LHGDN

A redundant oncogenic potential of the retinoic receptor (RAR) alpha, beta and gamma isoforms in acute promyelocytic leukemia.

17252005

2007

Entrez Id:	5914
Gene Symbol:	RARA

RARA

CUI:	C0023418
Disease:	leukemia

leukemia

0.100

GeneticVariation

LHGDN

Cytoplasmic function of mutant promyelocytic leukemia (PML) and PML-retinoic acid receptor-alpha.

16540467

2006

Entrez Id:	5914
Gene Symbol:	RARA

RARA

CUI:	C0023418
Disease:	leukemia

leukemia

0.100

Biomarker

LHGDN

Myeloid leukemia with promyelocytic features in transgenic mice expressing hCG-NuMA-RARalpha.

14737102

2004

Entrez Id:	5914
Gene Symbol:	RARA

RARA

CUI:	C0023418
Disease:	leukemia

leukemia

0.100

Biomarker

LHGDN

Two critical hits for promyelocytic leukemia.

11106752

2000