DisGeNET - a database of gene-disease associations

ILKAP, ILK associated serine/threonine phosphatase, 80895

N. diseases: 14; N. variants: 15

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:

rs12472274

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C0202177
Disease:

Phospholipid measurement

0.800

GeneticVariation

GWASDB

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

22359512

2012

dbSNP:

rs12472274

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C0202177
Disease:

Phospholipid measurement

0.800

GeneticVariation

GWASCAT

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

22359512

2012

dbSNP:

rs11677736

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs13020362

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs1374387

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs2278737

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs2880131

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs3795904

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs3795904

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs4663854

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs4663855

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs6431588

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs6722284

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs6749351

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs7598219

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

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:

rs35113840

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C0427460
Disease:

Red cell distribution width determination

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs35113840

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C1304746
Disease:

RDW - Red blood cell distribution width result

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs35676364

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C0524587
Disease:

Mean Corpuscular Volume (result)

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs35676364

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs6431588

Entrez Id:	80895
Gene Symbol:	ILKAP

ILKAP

CUI:	C0025202
Disease:

melanoma

0.010

GeneticVariation

BEFREE

Additionally, a second SNP (rs6431588) located on ILKAP was found to be associated with melanoma after considering a combined set of 1,883 MM cases and 1,358 disease-free controls.

24743186

2014