Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 51324
Gene Symbol: SPG21
SPG21
0.110 GeneticVariation disease BEFREE Maspardin is mutated in mast syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. 14564668 2003
Entrez Id: 51324
Gene Symbol: SPG21
SPG21
0.110 GeneticVariation disease LHGDN This frameshift results in the premature termination (fs201-212X213) of the encoded product, which is designated "maspardin" (Mast syndrome, spastic paraplegia, autosomal recessive with dementia), and has been shown elsewhere to localize to intracellular endosomal/trans-Golgi transportation vesicles and may function in protein transport and sorting. 14564668 2003
Entrez Id: 51324
Gene Symbol: SPG21
SPG21
0.110 Biomarker disease HPO