DisGeNET - a database of gene-disease associations

ST6GALNAC5, ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5, 81849

N. diseases: 23; N. variants: 7

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:

rs10873925

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0202236
Disease:

Triglycerides measurement

0.700

GeneticVariation

GWASCAT

Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.

30108155

2018

dbSNP:

rs12065122

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs4949764

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs6603933

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs6663942

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs17368584

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C0220650
Disease:

Metastatic malignant neoplasm to brain

0.010

GeneticVariation

BEFREE

ST6GALNAC5 rs17368584 and ITGB3 rs3809865 were significantly associated with BM susceptibility.

26689941

2017

dbSNP:

rs1206787329

Entrez Id:	81849
Gene Symbol:	ST6GALNAC5

ST6GALNAC5

CUI:	C1956346
Disease:

Coronary Artery Disease

0.010

GeneticVariation

BEFREE

A p.Val99Met causing mutation in ST6GALNAC5 was considered the likely cause of CAD.

24399302

2014