BAIT
SPG20
SPARTIN, TAHCCP1
spastic paraplegia 20 (Troyer syndrome)
GO Process (3)
GO Function (2)
GO Component (4)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
TUBA1A
B-ALPHA-1, LIS3, TUBA3
tubulin, alpha 1a
GO Process (8)
GO Function (2)
GO Component (6)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
FRET
An interaction is inferred when close proximity of interaction partners is detected by fluorescence resonance energy transfer between pairs of fluorophore-labeled molecules, such as occurs between CFP (donor) and YFP (acceptor) fusion proteins.
Publication
The hereditary spastic paraplegia protein spartin localises to mitochondria.
Hereditary spastic paraplegia describes a diverse group of disorders characterized by progressive paraparesis primarily affecting lower limbs. In Troyer syndrome, an autosomal recessive form of hereditary spastic paraplegia, patients have dysarthria, distal amyotrophy, developmental delay and short stature in addition to spastic paraparesis. It is caused by a frameshift mutation (1110delA) in SPG20 leading to premature truncation of spartin, a ... [more]
J. Neurochem. Sep. 01, 2006; 98(6);1908-19 [Pubmed: 16945107]
Throughput
- Low Throughput
Curated By
- BioGRID