neurodegeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment of function or destruction of neural tissue (Mammalian Phenotype Ontology, MP_0002229)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002180
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Genes

16 genes associated with the neurodegeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AARS2 alanyl-tRNA synthetase 2, mitochondrial
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
FOLR1 folate receptor 1 (adult)
GALC galactosylceramidase
GUSB glucuronidase, beta
IDS iduronate 2-sulfatase
IDUA iduronidase, alpha-L-
LYST lysosomal trafficking regulator
MFSD8 major facilitator superfamily domain containing 8
NBN nibrin
PANK2 pantothenate kinase 2
PCNA proliferating cell nuclear antigen
PDHA1 pyruvate dehydrogenase (lipoamide) alpha 1
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
TTC19 tetratricopeptide repeat domain 19
ZBTB20 zinc finger and BTB domain containing 20