cerebral degeneration Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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Genes

28 genes involed in the disease cerebral degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
AIMP1 aminoacyl tRNA synthetase complex-interacting multifunctional protein 1
ARSA arylsulfatase A
ARSB arylsulfatase B
ASPA aspartoacylase
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
FA2H fatty acid 2-hydroxylase
FAM126A family with sequence similarity 126, member A
GALC galactosylceramidase
GFAP glial fibrillary acidic protein
GJC2 gap junction protein, gamma 2, 47kDa
GLB1 galactosidase, beta 1
GM2A GM2 ganglioside activator
HEXA hexosaminidase A (alpha polypeptide)
HEXB hexosaminidase B (beta polypeptide)
HSPD1 heat shock 60kDa protein 1 (chaperonin)
LMNB1 lamin B1
NOTCH3 notch 3
PLP1 proteolipid protein 1
POLG polymerase (DNA directed), gamma
POLR3A polymerase (RNA) III (DNA directed) polypeptide A, 155kDa
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
PSAP prosaposin
SUMF1 sulfatase modifying factor 1