DisGeNET - a database of gene-disease associations

GREM2, gremlin 2, DAN family BMP antagonist, 64388

N. diseases: 22; N. variants: 6

Disease: TOOTH AGENESIS, SELECTIVE, 9 ×

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs373941682

rs373941682

Entrez Id:	64388
Gene Symbol:	GREM2

GREM2

CUI:	C4310638
Disease:

TOOTH AGENESIS, SELECTIVE, 9

0.800

GeneticVariation

UNIPROT

GREMLIN 2 Mutations and Dental Anomalies.

2015

dbSNP:

rs1057519288

rs1057519288

Entrez Id:	64388
Gene Symbol:	GREM2

GREM2

CUI:	C4310638
Disease:

TOOTH AGENESIS, SELECTIVE, 9

A

0.800

CausalMutation

CLINVAR

dbSNP:

rs1057519288

rs1057519288

Entrez Id:	64388
Gene Symbol:	GREM2

GREM2

CUI:	C4310638
Disease:

TOOTH AGENESIS, SELECTIVE, 9

0.800

GeneticVariation

UNIPROT

dbSNP:

rs373941682

rs373941682

Entrez Id:	64388
Gene Symbol:	GREM2

GREM2

CUI:	C4310638
Disease:

TOOTH AGENESIS, SELECTIVE, 9

A

0.800

CausalMutation

CLINVAR

dbSNP:

rs142343894

rs142343894

Entrez Id:	64388
Gene Symbol:	GREM2

GREM2

CUI:	C4310638
Disease:

TOOTH AGENESIS, SELECTIVE, 9

0.700

GeneticVariation

UNIPROT

GREMLIN 2 Mutations and Dental Anomalies.

2015