×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
CLINVAR
Comprehensive genomic analysis of patients with disorders of cerebral cortical development.
29706646
2018
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
27292316
2016
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders.
12552055
2003
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
12390976
2002
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.
11175293
2001
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Mutation of the doublecortin gene in male patients with double cortex syndrome: somatic mosaicism detected by hair root analysis.
11601509
2001
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Incomplete penetrance with normal MRI in a woman with germline mutation of the DCX gene.
11468322
2001
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
10807542
2000
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
BEFREE
Mutations in the X-linked gene doublecortin lead to "double cortex" syndrome (DC) in females and to X-linked lissencephaly (XLIS ) in males.
10915612
2000
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.
9989615
1999
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia.
10369164
1999
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
10441340
1999
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Deletions or mutations of LIS1 on 17p13.3 and mutations in XLIS ( DCX ) on Xq22.3-q23 produce LIS.
9817918
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
9668176
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
Biomarker
disease
BEFREE
We identified a novel 10 kb brain-specific cDNA interrupted by a balanced translocation in an XLIS patient that encodes a novel 40 kDa predicted protein named Doublecortin .
9489700
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
We identified a novel 10 kb brain-specific cDNA interrupted by a balanced translocation in an XLIS patient that encodes a novel 40 kDa predicted protein named Doublecortin .
9489700
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
9489699
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
Biomarker
disease
GENOMICS_ENGLAND
We identified a novel 10 kb brain-specific cDNA interrupted by a balanced translocation in an XLIS patient that encodes a novel 40 kDa predicted protein named Doublecortin .
9489700
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
BEFREE
Deletions or mutations of LIS1 on 17p13.3 and mutations in XLIS ( DCX ) on Xq22.3-q23 produce LIS.
9817918
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
GeneticVariation
disease
UNIPROT
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).
9618162
1998
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
CausalMutation
disease
CLINVAR
×
Entrez Id:
1641
Gene Symbol:
DCX
DCX
0.730
Biomarker
disease
CTD_human