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schizophrenia
Summary
- Synonym
-
- schizophrenia-1
- Definition
- A psychotic disorder that is characterized by a disintegration of thought processes and of emotional responsiveness.
- Super Class
- psychotic disorder
External Links
- Disease Ontology
- DOID:5419
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- MGI genotype (from TogoID)
-
- 5521202
- 5694657
- 5689835
- 5689331
- 5661067
- 5660929
- 5620953
- 5574284
- 5559028
- 5694660
- 5519120
- 5486680
- 5486142
- 5485349
- 5485273
- 5465282
- 5462366
- 5444462
- 6189180
- 7378550
- 6828730
- 6810192
- 6423106
- 6315641
- 6294898
- 6283412
- 6189202
- 5428448
- 5800496
- 5790635
- 5784537
- 5776380
- 5762957
- 5752786
- 5699086
- 3606460
- 3720943
- 3713111
- 3707975
- 3623286
- 3623253
- 3606731
- 3606703
- 3606580
- 3758089
- 3579532
- 3530740
- 3530450
- 3041140
- 2674288
- 2663269
- 2654500
- 4358724
- 5428306
- 5428133
- 5293444
- 5285873
- 5085985
- 5085920
- 4843272
- 4438921
- 2175046
- 4354165
- 4353812
- 3841583
- 3819267
- 3818698
- 3806713
- 3785829
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 10678 | B3GNT2 | UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 | |
| 10682 | EBP | EBP cholestenol delta-isomerase | |
| 10728 | PTGES3 | prostaglandin E synthase 3 | |
| 10998 | SLC27A5 | solute carrier family 27 member 5 | |
| 11332 | ACOT7 | acyl-CoA thioesterase 7 | |
| 22854 | NTNG1 | netrin G1 | |
| 22901 | ARSG | arylsulfatase G | |
| 23236 | PLCB1 | phospholipase C beta 1 | |
| 23275 | POFUT2 | protein O-fucosyltransferase 2 | |
| 23305 | ACSL6 | acyl-CoA synthetase long chain family member 6 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 11651 | Akt1 | thymoma viral proto-oncogene 1 | |
| 12654 | Chi3l1 | chitinase 3 like 1 | |
| 12846 | Comt | catechol-O-methyltransferase | |
| 15558 | Htr2a | 5-hydroxytryptamine (serotonin) receptor 2A | |
| 19013 | Ppara | peroxisome proliferator activated receptor alpha | |
| 21926 | Tnf | tumor necrosis factor | |
| 53374 | Chst3 | carbohydrate sulfotransferase 3 | |
| 56637 | Gsk3b | glycogen synthase kinase 3 beta | |
| 140481 | Man2a2 | mannosidase 2, alpha 2 | |
| 280645 | B3gat2 | beta-1,3-glucuronyltransferase 2 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 24185 | Akt1 | AKT serine/threonine kinase 1 | |
| 24267 | Comt | catechol-O-methyltransferase | |
| 24835 | Tnf | tumor necrosis factor | |
| 25747 | Ppara | peroxisome proliferator activated receptor alpha | |
| 29595 | Htr2a | 5-hydroxytryptamine receptor 2A | |
| 64544 | B3gat2 | beta-1,3-glucuronyltransferase 2 | |
| 84027 | Gsk3b | glycogen synthase kinase 3 beta | |
| 84468 | Chst3 | carbohydrate sulfotransferase 3 | |
| 89824 | Chi3l1 | chitinase 3 like 1 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 41126 | alpha-Man-IIa | alpha-Mannosidase class II a | |
| 251900 | GlcAT-I | Glucuronyltransferase I |
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 399170 | akt1.S | AKT serine/threonine kinase 1 S homeolog | Xenopus laevis (African clawed frog) | |
| 594928 | b3gat2 | beta-1,3-glucuronyltransferase 2 | Xenopus tropicalis (tropical clawed frog) | |
| 733177 | b3gat2.S | beta-1,3-glucuronyltransferase 2 S homeolog | Xenopus laevis (African clawed frog) | |
| 100492673 | chst3 | carbohydrate (chondroitin 6) sulfotransferase 3 | Xenopus tropicalis (tropical clawed frog) | |
| 108716933 | b3gat2.L | beta-1,3-glucuronyltransferase 2 L homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P08571 | Monocyte differentiation antigen CD14 | |
| P08842 | Steryl-sulfatase | |
| P09104 | Gamma-enolase | |
| P09326 | CD48 antigen | |
| P09382 | Galectin-1 | |
| P09467 | Fructose-1,6-bisphosphatase 1 | |
| P09622 | Dihydrolipoyl dehydrogenase, mitochondrial | |
| P09848 | Lactase/phlorizin hydrolase | |
| P09874 | Poly [ADP-ribose] polymerase 1 | |
| P09972 | Fructose-bisphosphate aldolase C |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002353 | EEG abnormality |
| HP:0000738 | Hallucinations |
| HP:0100753 | Schizophrenia |
| HP:0000006 | Autosomal dominant inheritance |
| HP:0007086 | Social and occupational deterioration |
| HP:0000746 | Delusion |
