Minimal Hepatic Encephalopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C3888788
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Genes

31 genes associated with the disease Minimal Hepatic Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ALB albumin
BDNF brain-derived neurotrophic factor
CAMK4 calcium/calmodulin-dependent protein kinase IV
CD69 CD69 molecule
CHAT choline O-acetyltransferase
CHRM1 cholinergic receptor, muscarinic 1
CREB1 cAMP responsive element binding protein 1
CX3CL1 chemokine (C-X3-C motif) ligand 1
DLG4 discs, large homolog 4 (Drosophila)
FBLIM1 filamin binding LIM protein 1
FZD2 frizzled class receptor 2
GLUL glutamate-ammonia ligase
GOPC golgi-associated PDZ and coiled-coil motif containing
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
IGF1 insulin-like growth factor 1 (somatomedin C)
IL15 interleukin 15
IL6 interleukin 6
JAK2 Janus kinase 2
NR4A3 nuclear receptor subfamily 4, group A, member 3
OSCP1 organic solute carrier partner 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
PTEN phosphatase and tensin homolog
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TAAR1 trace amine associated receptor 1
TNF tumor necrosis factor
WNT5A wingless-type MMTV integration site family, member 5A