DisGeNET - a database of gene-disease associations

Acylcarnitines measurement, C0523446

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:	5481
Gene Symbol:	PPID

PPID

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015

Entrez Id:	6583
Gene Symbol:	SLC22A4

SLC22A4

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015

Entrez Id:	33
Gene Symbol:	ACADL

ACADL

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015

Entrez Id:	220963
Gene Symbol:	SLC16A9

SLC16A9

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015

Entrez Id:	85413
Gene Symbol:	SLC22A16

SLC22A16

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015

Entrez Id:	553103
Gene Symbol:	MIR3936HG

MIR3936HG

0.100

GeneticVariation

phenotype

GWASCAT

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.

26068415

2015