DisGeNET - a database of gene-disease associations

CNTN4, contactin 4, 152330

N. diseases: 58; N. variants: 26

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:

rs11713158

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0021704
Disease:

Intelligence

0.800

GeneticVariation

GWASCAT

Genome-wide association study of intelligence: additive effects of novel brain expressed genes.

22449649

2012

dbSNP:

rs11713158

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0021704
Disease:

Intelligence

0.800

GeneticVariation

GWASDB

Genome-wide association study of intelligence: additive effects of novel brain expressed genes.

22449649

2012

dbSNP:

rs6781149

Entrez Id:	152330;105376926
Gene Symbol:	CNTN4;LOC105376926

CNTN4;LOC105376926

CUI:	C0021704
Disease:

Intelligence

0.800

GeneticVariation

GWASCAT

Genome-wide association study of intelligence: additive effects of novel brain expressed genes.

22449649

2012

dbSNP:

rs6781149

Entrez Id:	152330;105376926
Gene Symbol:	CNTN4;LOC105376926

CNTN4;LOC105376926

CUI:	C0021704
Disease:

Intelligence

0.800

GeneticVariation

GWASDB

Genome-wide association study of intelligence: additive effects of novel brain expressed genes.

22449649

2012

dbSNP:

rs9849237

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0220641
Disease:

Lip and Oral Cavity Carcinoma

0.710

GeneticVariation

BEFREE

Our data indicated genotypes and alleles in specific SNPs rs9849237, rs243865 and rs10090787 with increased/decreased risk to oral cancer.

28595731

2017

dbSNP:

rs9849237

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0220641
Disease:

Lip and Oral Cavity Carcinoma

0.710

GeneticVariation

CLINVAR

dbSNP:

rs11708578

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.

30285260

2019

dbSNP:

rs17194490

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study.

31268507

2019

dbSNP:

rs4561819

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.

31374203

2019

dbSNP:

rs4561819

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0021704
Disease:

Intelligence

0.700

GeneticVariation

GWASCAT

Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways.

31374203

2019

dbSNP:

rs66492629

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.

30285260

2019

dbSNP:

rs6768500

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C4268744
Disease:

Atypical femoral fracture

0.700

GeneticVariation

GWASCAT

A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture.

31006051

2019

dbSNP:

rs76646538

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C4268744
Disease:

Atypical femoral fracture

0.700

GeneticVariation

GWASCAT

A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture.

31006051

2019

dbSNP:

rs13071423

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Genomic atlas of the human plasma proteome.

29875488

2018

dbSNP:

rs163352

Entrez Id:	152330;100873975
Gene Symbol:	CNTN4;CNTN4-AS1

CNTN4;CNTN4-AS1

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Genomic atlas of the human plasma proteome.

29875488

2018

dbSNP:

rs163574

Entrez Id:	152330;100873975
Gene Symbol:	CNTN4;CNTN4-AS1

CNTN4;CNTN4-AS1

CUI:	C0200641
Disease:

Blood basophil count (lab test)

0.700

GeneticVariation

GWASCAT

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

29403010

2018

dbSNP:

rs17022006

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.

29503163

2018

dbSNP:

rs34877519

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs35346733

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

29483656

2018

dbSNP:

rs9845120

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs9858503

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs11708578

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia.

28991256

2017

dbSNP:

rs17194490

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0008074
Disease:

Child Development Disorders, Pervasive

0.700

GeneticVariation

GWASCAT

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

28540026

2017

dbSNP:

rs17194490

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0036341
Disease:

Schizophrenia

0.700

GeneticVariation

GWASCAT

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

28540026

2017

dbSNP:

rs41526344

Entrez Id:	152330
Gene Symbol:	CNTN4

CNTN4

CUI:	C0024117
Disease:

Chronic Obstructive Airway Disease

0.700

GeneticVariation

GWASCAT

Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1.

28044437

2017