Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. 10610178

1999
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. 10699187

2000
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia. 10699187

2000
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. 11309678

2001
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia. 11309678

2001
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation. 14681884

2003
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation. 14681884

2003
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene. 15326248

2004
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene. 15326248

2004
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia. 17100993

2006
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. 17101632

2006
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia. 17100993

2006
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. 17101632

2006
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia. 18190593

2008
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia. 18190593

2008
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients. 19453301

2009
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients. 19453301

2009
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations. 20562464

2010
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations. 20562464

2010
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance. 22554690

2012
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Normal spastin gene dosage is specifically required for axon regeneration. 23122959

2012
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance. 22554690

2012
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 CausalMutation CLINVAR Normal spastin gene dosage is specifically required for axon regeneration. 23122959

2012
Entrez Id: 6683
Gene Symbol: SPAST
SPAST
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.110 GeneticVariation CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886

2013