Pelger-Huet Anomaly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_9631)
External Link https://www.disgenet.org/browser/0/1/0/C0030779
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Genes

25 genes associated with the disease Pelger-Huet Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALAD aminolevulinate dehydratase
ASIC5 acid sensing (proton gated) ion channel family member 5
CA12 carbonic anhydrase XII
GH1 growth hormone 1
GORASP1 golgi reassembly stacking protein 1, 65kDa
HMBS hydroxymethylbilane synthase
IL1A interleukin 1, alpha
IL2 interleukin 2
LBR lamin B receptor
LMNA lamin A/C
MARS1 methionyl-tRNA synthetase 1
MPO myeloperoxidase
NBAS neuroblastoma amplified sequence
NR3C2 nuclear receptor subfamily 3, group C, member 2
POMC proopiomelanocortin
RELA v-rel avian reticuloendotheliosis viral oncogene homolog A
REN renin
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SELENBP1 selenium binding protein 1
SYT1 synaptotagmin I
TNF tumor necrosis factor
TP53 tumor protein p53
WNK1 WNK lysine deficient protein kinase 1