Congenital Pain Insensitivity Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0002768
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Genes

14 genes associated with the disease Congenital Pain Insensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARL6IP1 ADP-ribosylation factor-like 6 interacting protein 1
CLTCL1 clathrin, heavy chain-like 1
LIFR leukemia inhibitory factor receptor alpha
NAA50 N(alpha)-acetyltransferase 50, NatE catalytic subunit
NGF nerve growth factor (beta polypeptide)
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
POMC proopiomelanocortin
PRDM12 PR domain containing 12
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN11A sodium channel, voltage gated, type XI alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
TAC1 tachykinin, precursor 1
TRPA1 transient receptor potential cation channel, subfamily A, member 1
WNK1 WNK lysine deficient protein kinase 1