×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Spinocerebellar Ataxia Type 6 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
27476654
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Spinocerebellar Ataxia Type 6 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy.
27250579
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy.
27250579
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
27476654
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Spinocerebellar Ataxia Type 6 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
21734179
2011
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
21734179
2011
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2 ).
19182766
2009
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Spinocerebellar Ataxia Type 6 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Spinocerebellar Ataxia Type 6 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Episodic ataxia type 2 (disorder)
1.000
Biomarker
GENOMICS_ENGLAND
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine.
12756131
2003
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
Biallelic CACNA1A mutations cause early onset epileptic encephalopathy with progressive cerebral, cerebellar, and optic nerve atrophy.
27250579
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
27476654
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias.
21734179
2011
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Hemiplegic migraine, familial type 1
0.800
Biomarker
GENOMICS_ENGLAND
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
8898206
1996
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Absence Epilepsy
0.760
Biomarker
GENOMICS_ENGLAND
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
8898206
1996
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
0.700
Biomarker
GENOMICS_ENGLAND
De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.
27476654
2016
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
0.700
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
0.700
Biomarker
GENOMICS_ENGLAND
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4.
8898206
1996
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Dystonia
0.480
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Dystonia
0.480
Biomarker
GENOMICS_ENGLAND
Primary episodic ataxias: diagnosis, pathogenesis and treatment.
17575281
2007
×
Entrez Id:
773
Gene Symbol:
CACNA1A
CACNA1A
Dystonia
0.480
Biomarker
GENOMICS_ENGLAND