DisGeNET - a database of gene-disease associations

DCX, doublecortin, 1641

N. diseases: 175; N. variants: 107

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:

rs104894779

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894779

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894780

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs104894780

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894780

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894781

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894781

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs104894781

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894782

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs104894782

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894782

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894783

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs104894783

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894783

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894784

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894784

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894785

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs104894785

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs104894786

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs122457137

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

11175293

2001

dbSNP:

rs122457137

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs122457137

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.

11601509

2001

dbSNP:

rs56030372

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.

11468322

2001

dbSNP:

rs104894779

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.

10807542

2000

dbSNP:

rs104894780

Entrez Id:	1641
Gene Symbol:	DCX

DCX

CUI:	C4551968
Disease:

Lissencephaly, X-Linked, 1

0.800

GeneticVariation

UNIPROT

Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.

10807542

2000