DisGeNET - a database of gene-disease associations

DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101

Disease: MIRROR MOVEMENTS 1 ×

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

Disease

Score _gda

Association Type

Type

Original DB

Sentence supporting the association

PMID

PMID Year

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

GeneticVariation

phenotype

UNIPROT

Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

28250454

2017

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

GeneticVariation

phenotype

UNIPROT

Mutations in DCC cause congenital mirror movements.

20431009

2010

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

CausalMutation

phenotype

CLINVAR

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

Biomarker

phenotype

GENOMICS_ENGLAND

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

Biomarker

phenotype

GENOMICS_ENGLAND

CUI:	C1834870
Disease:	MIRROR MOVEMENTS 1

MIRROR MOVEMENTS 1

0.700

Biomarker

phenotype

CTD_human