Fatal Familial Insomnia 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_0050433)
External Link https://www.disgenet.org/browser/0/1/0/C0206042
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Genes

24 genes associated with the disease Fatal Familial Insomnia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
AQP1 aquaporin 1 (Colton blood group)
C4BPA complement component 4 binding protein, alpha
CARD14 caspase recruitment domain family, member 14
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
COX2
CSNK2A2 casein kinase 2, alpha prime polypeptide
GFAP glial fibrillary acidic protein
GH1 growth hormone 1
GLS glutaminase
MDH1 malate dehydrogenase 1, NAD (soluble)
MLKL mixed lineage kinase domain-like
MPRIP myosin phosphatase Rho interacting protein
NDUFB8 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 8, 19kDa
PRDX2 peroxiredoxin 2
PRL prolactin
PRNP prion protein
RASA2 RAS p21 protein activator 2
RIPK3 receptor-interacting serine-threonine kinase 3
RYR2 ryanodine receptor 2 (cardiac)
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
TSPO translocator protein (18kDa)
UQCRC2 ubiquinol-cytochrome c reductase core protein II
ZBTB38 zinc finger and BTB domain containing 38