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DISEASES
The following proteins in
Homo sapiens
appear to match your input.
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1) '9606.ENSP00000261707':
SLC6A4 - Sodium-dependent serotonin transporter; Serotonin transporter whose primary function in the central nervous system involves the regulation of serotonergic signaling via transport of serotonin molecules from the synaptic cleft back into the pre-synaptic terminal for re-utilization. Plays a key role in mediating regulation of the availability of serotonin to other receptors of serotonergic systems. Terminates the action of serotonin and recycles it in a sodium-dependent manner.
[a.k.a. CCDS11256, NM_001045, ENST00000394821]
2) '9606.ENSP00000340684':
MAOA - Amine oxidase [flavin-containing] A; Catalyzes the oxidative deamination of biogenic and xenobiotic amines and has important functions in the metabolism of neuroactive and vasoactive amines in the central nervous system and peripheral tissues. MAOA preferentially oxidizes biogenic amines such as 5-hydroxytryptamine (5-HT), norepinephrine and epinephrine.
[a.k.a. OTTHUMG00000021387, ENSP00000340684, EC 1.4.3.4]
3) '9606.ENSP00000361646':
ZMYND12 - Zinc finger MYND-type containing 12.
[a.k.a. ENSG00000066185, ENSP00000355404, NM_032257]
4) '9606.PARD6G-AS1':
- - Sorry, STRING found no proteins by this name in Homo sapiens - -
5) '9606.ENSP00000437737':
HTR2A - 5-hydroxytryptamine receptor 2A; G-protein coupled receptor for 5-hydroxytryptamine (serotonin). Also functions as a receptor for various drugs and psychoactive substances, including mescaline, psilocybin, 1-(2,5-dimethoxy-4-iodophenyl)-2- aminopropane (DOI) and lysergic acid diethylamide (LSD). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors. Beta-arrestin family members inhibit signaling via G proteins and mediate activation of alternative signaling pathways. S [...]
[a.k.a. R-HSA-388396, AAH74848.1, R-HSA-162582]
6) '9606.ENSP00000354511':
COMT - Catechol O-methyltransferase; Catalyzes the O-methylation, and thereby the inactivation, of catecholamine neurotransmitters and catechol hormones. Also shortens the biological half-lives of certain neuroactive drugs, like L-DOPA, alpha-methyl DOPA and isoproterenol; Belongs to the class I-like SAM-binding methyltransferase superfamily. Cation-dependent O-methyltransferase family.
[a.k.a. ENSP00000385150, uc002zqu.4, 4XUC]
7) '9606.ENSP00000217386':
OXT - Oxytocin-neurophysin 1; Neurophysin 1 specifically binds oxytocin.
[a.k.a. R-HSA-388396, Oxytocin/neurophysin I prepropeptide, AAA59979.1]
8) '9606.ENSP00000354859':
DRD2 - D(2) dopamine receptor; Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase; Belongs to the G-protein coupled receptor 1 family.
[a.k.a. ENST00000355319, AF176812, R-HSA-162582]
9) '9606.ENSP00000358963':
HTR1B - 5-hydroxytryptamine receptor 1B; G-protein coupled receptor for 5-hydroxytryptamine (serotonin). Also functions as a receptor for ergot alkaloid derivatives, various anxiolytic and antidepressant drugs and other psychoactive substances, such as lysergic acid diethylamide (LSD). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Signaling inhibits adenylate cyclase activity. Arrestin family members inhibit signaling via G proteins and medi [...]
[a.k.a. R-HSA-388396, ENSG00000135312, R-HSA-162582]
10) '9606.ENSP00000316244':
HTR1A - 5-hydroxytryptamine receptor 1A; G-protein coupled receptor for 5-hydroxytryptamine (serotonin). Also functions as a receptor for various drugs and psychoactive substances. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of down-stream effectors, such as adenylate cyclase. Beta-arrestin family members inhibit signaling via G proteins and mediate activation of alternative signaling pathways. Signaling inhibits adenylate cyclase activity and activates a phosphatidylinositol-calcium second [...]
[a.k.a. R-HSA-388396, CAA40962.1, R-HSA-162582]
