Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease BEFREE Here, we review the physiological roles of AGC1, its links to calcium homeostasis, and its involvement in autism pathogenesis. 21691713 2011
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease BEFREE Our data do not support that the SLC25A12 gene is associated with autism in our population. 19913066 2010
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE Association between autism and single-nucleotide polymorphisms in SLC25A12 has been reported in various studies. 18180767 2008
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease CTD_human An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. 18348195 2008
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE This study shows further support that genetic variants within SLC25A12 gene contribute to the etiology of autism. 19360665 2008
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. 17894412 2008
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE In the past this gene has been found to be associated with susceptibility to autism; in this study we tested the hypothesis that SLC25A12 genetic variants confer susceptibility to schizophrenia. 17693006 2007
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE Recently, significant association with autism has been reported for single-nucleotide polymorphisms (SNPs) in the SLC25A12 and CMYA3 genes on chromosome 2q. 16205742 2006
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease BEFREE These results suggest that SLC25A12 is not a major contributor to autism risk in these families. 16648338 2006
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 GeneticVariation disease BEFREE We conclude that while mitochondrial dysfunction may be one of the most common medical conditions associated with autism, variation at the SLC25A12 gene does not explain the high frequency of mitochondrial dysfunction markers and is not associated with autism in this sample of autistic patients. 17151801 2006
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease BEFREE These findings provide replication of the association between autism and SLC25A12. 16263864 2005
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease BEFREE Further studies are needed to confirm this association and to decipher any potential etiological role of AGC1 in autism. 15056512 2004
Entrez Id: 8604
Gene Symbol: SLC25A12
SLC25A12
0.400 Biomarker disease CTD_human Linkage and association were observed between autistic disorder and the two SNPs, rs2056202 and rs2292813, found in SLC25A12. 15056512 2004