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Standards Ontologies Notations
Guidelines
MIRAGE
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
Disease Ontology
DOID:5419
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 57 in total
Gene ID Gene Symbol Description Source
1822 ATN1 atrophin 1
2571 GAD1 glutamate decarboxylase 1
2572 GAD2 glutamate decarboxylase 2
2893 GRIA4 glutamate ionotropic receptor AMPA type subunit 4
2903 GRIN2A glutamate ionotropic receptor NMDA type subunit 2A
2904 GRIN2B glutamate ionotropic receptor NMDA type subunit 2B
2918 GRM8 glutamate metabotropic receptor 8
2932 GSK3B glycogen synthase kinase 3 beta
3303 HSPA1A heat shock protein family A (Hsp70) member 1A
3304 HSPA1B heat shock protein family A (Hsp70) member 1B
Displaying entries 1 - 10 of 32 in total
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
Displaying all 3 entries
Gene ID Gene Symbol Description Source
24598 Nos1 nitric oxide synthase 1
25248 Cnr1 cannabinoid receptor 1
29595 Htr2a 5-hydroxytryptamine receptor 2A
Displaying 1 entry
Gene ID Gene Symbol Description Source
47220 Fur1 Furin 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
403310 cacna1da calcium channel, voltage-dependent, L type, alpha 1D subunit, a
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
P30430 Furin-like protease 1, isoform 1-CRR
The Human Phenotype Ontology
Displaying all 6 entries
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
Displaying all 3 entries
Gene ID Gene Symbol Description
1312 COMT catechol-O-methyltransferase
65078 RTN4R reticulon 4 receptor
1116 CHI3L1 chitinase 3 like 1
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025