Morphine Dependence Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An opiate dependence that involves the continued use of morphine despite despite problems related to use of the substance. (Human Disease Ontology, DOID_2560)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009021
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Genes

15 genes/proteins associated with the disease Morphine Dependence from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
OPRM1 opioid receptor, mu 1 2.88009
OPRL1 opiate receptor-like 1 2.88009
GRIA1 glutamate receptor, ionotropic, AMPA 1 2.88009
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A 2.88009
CREB1 cAMP responsive element binding protein 1 2.88009
NOS1 nitric oxide synthase 1 (neuronal) 2.88009
MMP9 matrix metallopeptidase 9 2.88009
POMC proopiomelanocortin 1.28456
OPRK1 opioid receptor, kappa 1 1.24213
PRL prolactin 1.17497
OPRD1 opioid receptor, delta 1 1.13279
GFAP glial fibrillary acidic protein 1.10872
MAPK1 mitogen-activated protein kinase 1 1.08407
NOS2 nitric oxide synthase 2, inducible 1.05573
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 1.04538