Miosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Abnormal (non-physiological) constriction of the pupil. (Human Phenotype Ontology, HP_0000616)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D015877
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Genes

31 genes/proteins associated with the disease Miosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary) 2.88009
FOS FBJ murine osteosarcoma viral oncogene homolog 1.92532
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.63294
OPRM1 opioid receptor, mu 1 1.60594
BAX BCL2-associated X protein 1.53989
TH tyrosine hydroxylase 1.48273
ACHE acetylcholinesterase (Yt blood group) 1.41368
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 1.38696
CRH corticotropin releasing hormone 1.36961
NPY neuropeptide Y 1.35792
EGR1 early growth response 1 1.34955
PRL prolactin 1.3414
IL1B interleukin 1, beta 1.27905
MAPK3 mitogen-activated protein kinase 3 1.25713
MAPK1 mitogen-activated protein kinase 1 1.24812
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.2059
DRD2 dopamine receptor D2 1.20526
TNF tumor necrosis factor 1.16035
CHRM2 cholinergic receptor, muscarinic 2 1.14575
CALCA calcitonin-related polypeptide alpha 1.14473
CHRM4 cholinergic receptor, muscarinic 4 1.1253
BCHE butyrylcholinesterase 1.11431
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.10734
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1 1.09786
BCL2 B-cell CLL/lymphoma 2 1.09262
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.06588
DRD1 dopamine receptor D1 1.06152
JUN jun proto-oncogene 1.04978
BDNF brain-derived neurotrophic factor 1.04904
CHAT choline O-acetyltransferase 1.04684
POMC proopiomelanocortin 1.03939