Gene: CHCHD10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 Biomarker disease BEFREE Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice. 31690696 2020
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 GeneticVariation disease BEFREE Dominant mutations in CHCHD10 cause amyotrophic lateral sclerosis (ALS)/frontotemporal dementia, and mutations in CHCHD2 have been associated with Parkinson's disease, but the function of these proteins remains unknown. 29121267 2018
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 GeneticVariation disease BEFREE Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia. 28462717 2017
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 GeneticVariation disease BEFREE Mutations in CHCHD10 have recently been reported as a cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. 26344877 2015
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 Biomarker disease BEFREE A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. 24934289 2014
Entrez Id: 400916
Gene Symbol: CHCHD10
CHCHD10 		0.060 Biomarker disease BEFREE Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. 25155093 2014