Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease BEFREE An hsp60 D3G mutation leads to MitCHAP-60, an early onset neurodegenerative disease while hsp60 V72I has been linked to SPG13, a form of hereditary spastic paraplegia. 31444388 2019
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 Biomarker disease MGD Late onset motoneuron disorder caused by mitochondrial Hsp60 chaperone deficiency in mice. 23466696 2013
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 Biomarker disease BEFREE Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia. 19423133 2009
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease BEFREE Mutations in the HSPD1 gene that encodes Hsp60 have been identified in patients with an autosomal dominant form of hereditary spastic paraplegia (SPG13), a late-onset neurodegenerative disorder characterized by a progressive paraparesis of the lower limbs. 18378094 2008
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease BEFREE We have previously reported the association of a mutation (c.292G > A/p.V98I) in the human HSPD1 gene that encodes the mitochondrial Hsp60 chaperonin with a dominantly inherited form of hereditary spastic paraplegia. 18400758 2008
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease BEFREE In the present work we have investigated 23 Danish index patients with hereditary spastic paraplegia (HSP) for mutations in the HSPD1 gene. 17420924 2007
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease BEFREE Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60. 11898127 2002
Entrez Id: 3329
Gene Symbol: HSPD1
HSPD1
0.260 GeneticVariation disease LHGDN Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60. 11898127 2002