schizophrenia
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 51586 | MED15 | mediator complex subunit 15 | |
| 53335 | BCL11A | BCL11 transcription factor A | |
| 65078 | RTN4R | reticulon 4 receptor | |
| 84062 | DTNBP1 | dystrobrevin binding protein 1 | |
| 89781 | HPS4 | HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 | |
| 93986 | FOXP2 | forkhead box P2 | |
| 135152 | B3GAT2 | beta-1,3-glucuronyltransferase 2 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 11441 | Chrna7 | cholinergic receptor, nicotinic, alpha polypeptide 7 | |
| 11651 | Akt1 | thymoma viral proto-oncogene 1 | |
| 13032 | Ctsc | cathepsin C | |
| 13162 | Slc6a3 | solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 | |
| 14683 | Gnas | GNAS complex locus | |
| 14810 | Grin1 | glutamate receptor, ionotropic, NMDA1 (zeta 1) | |
| 15273 | Hivep2 | human immunodeficiency virus type I enhancer binding protein 2 | |
| 16569 | Kif3b | kinesin family member 3B | |
| 17760 | Map6 | microtubule-associated protein 6 | |
| 18189 | Nrxn1 | neurexin I |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P35372 | Mu-type opioid receptor | |
| P35462 | D(3) dopamine receptor | |
| P36222 | Chitinase-3-like protein 1 | |
| P48058 | Glutamate receptor 4 | |
| P49841 | Glycogen synthase kinase-3 beta | |
| P53708 | Integrin alpha-8 | |
| P54219 | Chromaffin granule amine transporter | |
| P54259 | Atrophin-1 | |
| Q03518 | Antigen peptide transporter 1 | |
| Q12879 | Glutamate receptor ionotropic, NMDA 2A |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P14842 | 5-hydroxytryptamine receptor 2A | |
| P20272 | Cannabinoid receptor 1 | |
| P29476 | Nitric oxide synthase 1 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| P30430 | Furin-like protease 1, isoform 1-CRR |
| UniProt ID | Protein Name | Source |
|---|---|---|
| A0A8M9Q738 | Voltage-dependent L-type calcium channel subunit alpha |
| HPO ID | HPO Term |
|---|---|
| HP:0000746 | Delusion |
| HP:0100753 | Schizophrenia |
| HP:0007086 | Social and occupational deterioration |
| HP:0000738 | Hallucinations |
| HP:0002353 | EEG abnormality |
| HP:0000006 | Autosomal dominant inheritance |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: August 4, 2025