×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
10699187
2000
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
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
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
Movement Disorders
0.110
GeneticVariation
CLINVAR
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia.
10699187
2000
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing.
26374131
2016
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
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
Movement Disorders
0.110
GeneticVariation
CLINVAR
Pathogenic mutation of spastin has gain-of-function effects on microtubule dynamics.
24478365
2014
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
26671083
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.
26208798
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.
26208798
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
A complex form of hereditary spastic paraplegia in three siblings due to somatic mosaicism for a novel SPAST mutation in the mother.
25315759
2014
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
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
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
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
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
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
Movement Disorders
0.110
CausalMutation
CLINVAR
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.
26671083
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
CausalMutation
CLINVAR
Hereditary spastic paraplegia SPG4: what is known and not known about the disease.
26094131
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Exome sequencing is a useful diagnostic tool for complicated forms of hereditary spastic paraplegia.
23438842
2014
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
Movement Disorders
0.110
GeneticVariation
CLINVAR
Hereditary spastic paraplegia SPG4: what is known and not known about the disease.
26094131
2015
×
Entrez Id:
6683
Gene Symbol:
SPAST
SPAST
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
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
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
Movement Disorders
0.110
GeneticVariation
CLINVAR
Hereditary spastic paraplegia in Greece: characterisation of a previously unexplored population using next-generation sequencing.
26374131
2016