rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Amyotrophic Lateral Sclerosis
0.010
GeneticVariation
BEFREE
Among the 4256 patients included in the analysis (2589 male [60.8%] and 1667 female [39.2%]; mean [SD] age at onset, 59 [12] years), the following 2 novel loci were significantly associated with ALS survival: at 10q23 (rs139550538; P = 1.87 × 10-9) and in the CAMTA1 gene at 1p36 (rs2412208 , P = 3.53 × 10-8).
27244217
2016
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
AMYOTROPHIC LATERAL SCLEROSIS 1
0.700
GeneticVariation
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
0.700
GeneticVariation
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.700
GeneticVariation
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
rs2412208
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Amyotrophic Lateral Sclerosis, Sporadic
0.700
GeneticVariation
GWASCAT
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.
27244217
2016
rs10864302
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Autosomal dominant compelling helio ophthalmic outburst syndrome
0.700
GeneticVariation
GWASCAT
Detection and interpretation of shared genetic influences on 42 human traits.
27182965
2016
rs12128526
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs1891215
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Body mass index
T
0.700
GeneticVariation
GWASCAT
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry.
30239722
2019
rs1135401818
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
24738973
2015
rs1553238311
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
A
0.700
GeneticVariation
CLINVAR
rs863224853
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION
G
0.700
GeneticVariation
CLINVAR
rs185305928
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Chemical and Drug Induced Liver Injury
0.700
GeneticVariation
GWASCAT
Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study.
28043905
2017
rs10864294
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Coronary Artery Disease
0.010
GeneticVariation
BEFREE
Exploration of the identified genes for the presence of disease associated variants, using Affymetrix 500K genotyping and Illumina custom genotyping arrays, highlighted a region upstream of VAMP3 within CAMTA1 to be associated with increased risk of CAD [rs10864294 P = 0.015, odds ratio (OR) = 1.30, 95% confidence interval (CI) = 1.1-1.6, 1471 cases, 2737 controls] and aggressive PD (AgP; P = 0.008, OR = 1.31, 95% CI = 1.1-1.6, 864 cases, 3664 controls).
23813974
2013
rs2301462
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Coronary Artery Disease
0.010
GeneticVariation
BEFREE
In silico replication in a meta-analysis of 14 genome-wide association studies of CAD of the CARDIoGRAM Consortium identified rs2301462 , located on the same haplotype block, as associated with P = 0.001 upon adjustment for sex and age.
23813974
2013
rs1193179
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASDB
Identification of susceptibility genes for complex diseases using pooling-based genome-wide association scans.
19184112
2009
rs1193179
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Diabetes Mellitus, Non-Insulin-Dependent
0.700
GeneticVariation
GWASDB
A genome-wide association study identifies novel risk loci for type 2 diabetes.
17293876
2007
rs4908678
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Diastolic blood pressure
T
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs7534398
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Duration of sleep
A
0.700
GeneticVariation
GWASCAT
Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates.
30846698
2019
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.
17470457
2007
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability.
22693284
2012
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
A potential dimerization region of dCAMTA is critical for termination of fly visual response.
17537720
2007
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
24738973
2015
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
The transcriptional coactivator CAMTA2 stimulates cardiac growth by opposing class II histone deacetylases.
16678093
2006
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation.
24145135
2014
rs1553238271
×
Entrez Id:
23261
Gene Symbol:
CAMTA1
CAMTA1
Dysmorphic features
T
0.700
GeneticVariation
CLINVAR
Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor.
25049392
2014