Polyneuropathy, Motor Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0271683
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Genes

32 genes associated with the disease Polyneuropathy, Motor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGRN agrin
AGTPBP1 ATP/GTP binding protein 1
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CHAT choline O-acetyltransferase
COL13A1 collagen, type XIII, alpha 1
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
EPO erythropoietin
GARS glycyl-tRNA synthetase
HINT1 histidine triad nucleotide binding protein 1
IGHMBP2 immunoglobulin mu binding protein 2
MYO9A myosin IXA
PMP22 peripheral myelin protein 22
PNPLA6 patatin-like phospholipase domain containing 6
POMC proopiomelanocortin
PPOX protoporphyrinogen oxidase
REEP1 receptor accessory protein 1
SCO2 SCO2 cytochrome c oxidase assembly protein
SCP2 sterol carrier protein 2
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SLC18A3 solute carrier family 18 (vesicular acetylcholine transporter), member 3
SLC25A1 solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7
SNAP25 synaptosomal-associated protein, 25kDa
SPG11 spastic paraplegia 11 (autosomal recessive)
SYT2 synaptotagmin II
TFG TRK-fused gene
TRPV4 transient receptor potential cation channel, subfamily V, member 4
TTR transthyretin
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)
WDHD1 WD repeat and HMG-box DNA binding protein 1