polyneuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001271
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Genes

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

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
APOA1 apolipoprotein A-I
ATP7B ATPase, Cu++ transporting, beta polypeptide
C4A complement component 4A (Rodgers blood group)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DGUOK deoxyguanosine kinase
DHH desert hedgehog
EDNRB endothelin receptor type B
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FAM126A family with sequence similarity 126, member A
FUCA1 fucosidase, alpha-L- 1, tissue
GCLC glutamate-cysteine ligase, catalytic subunit
GSN gelsolin
HLA-B major histocompatibility complex, class I, B
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
LDB3 LIM domain binding 3
MEFV Mediterranean fever
MYD88 myeloid differentiation primary response 88
MYOT myotilin
NLRP3 NLR family, pyrin domain containing 3
NOD2 nucleotide-binding oligomerization domain containing 2
PEX11B peroxisomal biogenesis factor 11 beta
PEX12 peroxisomal biogenesis factor 12
PMM2 phosphomannomutase 2
PRTN3 proteinase 3
PSAP prosaposin
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SEPT9 septin 9
SETX senataxin
SH3TC2 SH3 domain and tetratricopeptide repeats 2
SLC25A19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
SNAP29 synaptosomal-associated protein, 29kDa
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TTR transthyretin