Atrophy/Degeneration Affecting The Brainstem Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4024900
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Genes

27 genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
COG5 component of oligomeric golgi complex 5
COG8 component of oligomeric golgi complex 8
DEGS1 delta(4)-desaturase, sphingolipid 1
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
DNAJC3 DnaJ (Hsp40) homolog, subfamily C, member 3
DNM1L dynamin 1-like
DNMT1 DNA (cytosine-5-)-methyltransferase 1
FA2H fatty acid 2-hydroxylase
FARS2 phenylalanyl-tRNA synthetase 2, mitochondrial
KIF1A kinesin family member 1A
LY6E lymphocyte antigen 6 complex, locus E
MCOLN1 mucolipin 1
OPA1 optic atrophy 1 (autosomal dominant)
RARS2 arginyl-tRNA synthetase 2, mitochondrial
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SPTAN1 spectrin, alpha, non-erythrocytic 1
TBCD tubulin folding cofactor D
TBP TATA box binding protein
TRAPPC6B trafficking protein particle complex 6B
TRRAP transformation/transcription domain-associated protein
TWNK twinkle mtDNA helicase
ZNHIT3 zinc finger, HIT-type containing 3