Postmortem Changes Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

36 genes associated with the Postmortem Changes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ANKK1 ankyrin repeat and kinase domain containing 1
APOE apolipoprotein E
BDNF brain-derived neurotrophic factor
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
COMT catechol-O-methyltransferase
CYP46A1 cytochrome P450, family 46, subfamily A, polypeptide 1
DAOA D-amino acid oxidase activator
DISC1 disrupted in schizophrenia 1
DRD2 dopamine receptor D2
DSCAM Down syndrome cell adhesion molecule
FEZ1 fasciculation and elongation protein zeta 1 (zygin I)
GAB2 GRB2-associated binding protein 2
GABRB2 gamma-aminobutyric acid (GABA) A receptor, beta 2
GBA glucosidase, beta, acid
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B
HCAR2 hydroxycarboxylic acid receptor 2
HCAR3 hydroxycarboxylic acid receptor 3
LRRK2 leucine-rich repeat kinase 2
MC5R melanocortin 5 receptor
MCHR1 melanin-concentrating hormone receptor 1
MCHR2 melanin-concentrating hormone receptor 2
MIR137 microRNA 137
MT-ND2 MTND2
NDEL1 nudE neurodevelopment protein 1-like 1
NOS1 nitric oxide synthase 1 (neuronal)
NPY neuropeptide Y
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PDE4B phosphodiesterase 4B, cAMP-specific
RGS2 regulator of G-protein signaling 2
RPGRIP1L RPGRIP1-like
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC1A2 solute carrier family 1 (glial high affinity glutamate transporter), member 2
TDO2 tryptophan 2,3-dioxygenase
TPH2 tryptophan hydroxylase 2
ZNF804A zinc finger protein 804A