DLGAP2
geneOn this page
Also known as DAP-2
Summary
DLGAP2 (DLG associated protein 2, HGNC:2906) is a protein-coding gene on chromosome 8p23.3, encoding Disks large-associated protein 2 (Q9P1A6). May play a role in the molecular organization of synapses and neuronal cell signaling.
The product of this gene is a membrane-associated protein that may play a role in synapse organization and signalling in neuronal cells. This gene is biallelically expressed in the brain, however, only the paternal allele is expressed in the testis (PMID:18055845). Alternatively spliced transcript variants encoding different isoforms have been identified.
Source: NCBI Gene 9228 — RefSeq curated summary.
At a glance
- Gene–disease (curated): complex neurodevelopmental disorder (Limited, ClinGen)
- GWAS associations: 20
- Clinical variants (ClinVar): 260 total — 4 pathogenic, 1 likely-pathogenic
- Phenotypes (HPO): 1
- Dosage sensitivity (ClinGen): haploinsufficiency no evidence, triplosensitivity no evidence
- MANE Select transcript:
NM_001346810
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:2906 |
| Approved symbol | DLGAP2 |
| Name | DLG associated protein 2 |
| Location | 8p23.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | DAP-2 |
| Ensembl gene | ENSG00000198010 |
| Ensembl biotype | protein_coding |
| OMIM | 605438 |
| Entrez | 9228 |
Gene structure
Transcript identifiers
Ensembl transcripts: 15 — 8 protein_coding_CDS_not_defined, 6 protein_coding, 1 retained_intron
ENST00000421627, ENST00000518530, ENST00000520524, ENST00000520816, ENST00000520901, ENST00000522092, ENST00000522499, ENST00000522626, ENST00000522989, ENST00000524065, ENST00000524139, ENST00000577187, ENST00000578889, ENST00000612087, ENST00000637795
RefSeq mRNA: 1 — MANE Select: NM_001346810
NM_001346810
CCDS: CCDS87572
Canonical transcript exons
ENST00000620101 — 0 exons
Expression profiles
Bgee: expression breadth ubiquitous, 113 present calls, max score 90.26.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.9616 / max 110.0647, expressed in 117 samples.
FANTOM5 promoters (6 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 87141 | 0.5651 | 89 |
| 87142 | 0.3210 | 81 |
| 87143 | 0.0378 | 3 |
| 87144 | 0.0225 | 3 |
| 87161 | 0.0093 | 3 |
| 87162 | 0.0059 | 3 |
Top tissues by expression
125 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| left testis | UBERON:0004533 | 90.26 | gold quality |
| right testis | UBERON:0004534 | 89.40 | gold quality |
| testis | UBERON:0000473 | 89.23 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 85.09 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 83.94 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 82.03 | gold quality |
| primary visual cortex | UBERON:0002436 | 81.75 | gold quality |
| corpus callosum | UBERON:0002336 | 78.57 | gold quality |
| prefrontal cortex | UBERON:0000451 | 77.95 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 77.64 | gold quality |
| frontal cortex | UBERON:0001870 | 77.56 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 77.23 | gold quality |
| right frontal lobe | UBERON:0002810 | 76.39 | gold quality |
| cerebral cortex | UBERON:0000956 | 76.06 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 75.52 | gold quality |
| nucleus accumbens | UBERON:0001882 | 73.62 | gold quality |
| putamen | UBERON:0001874 | 72.30 | gold quality |
| Ammon’s horn | UBERON:0001954 | 71.33 | gold quality |
| caudate nucleus | UBERON:0001873 | 71.32 | gold quality |
| temporal lobe | UBERON:0001871 | 70.04 | gold quality |
| amygdala | UBERON:0001876 | 69.82 | gold quality |
| cortical plate | UBERON:0005343 | 69.53 | gold quality |
| brain | UBERON:0000955 | 68.83 | gold quality |
| pituitary gland | UBERON:0000007 | 68.80 | gold quality |
| adenohypophysis | UBERON:0002196 | 66.78 | gold quality |
| hypothalamus | UBERON:0001898 | 63.45 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 58.62 | gold quality |
| thyroid gland | UBERON:0002046 | 57.73 | gold quality |
| left lobe of thyroid gland | UBERON:0001120 | 57.53 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 56.73 | gold quality |
Single-cell (SCXA)
Detected in 5 experiment(s), a significant marker in 4.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-180759 | yes | 1517.76 |
| E-HCAD-30 | yes | 1449.47 |
| E-HCAD-25 | yes | 1417.30 |
| E-HCAD-35 | yes | 104.19 |
| E-ANND-3 | no | 1.56 |
Regulation
Is transcription factor: no
Functional genomics
ClinGen dosage: haploinsufficiency 0 (no evidence), triplosensitivity 0 (no evidence). ClinGen Gene Dosage Map
Literature-anchored findings (GeneRIF, showing 10)
- Increased expression of PSD-25 and its coassembly with NMDA-receptor subunits NR1 and MR2B in resected epileptic cortical tissue suggest a possible functional role of the complex in in situ epileptogenicity of focal cortical dysplasia. (PMID:15030493)
- DLGAP2 gene is imprinted, with preferential expression from the paternal allele in testis. (PMID:18055845)
- this study demonistrated that two SNPs in DLGAP2 (rs6558484 and rs7014992) and prefrontal cortex white matter volume. (PMID:23154099)
- DLGAP2 is a susceptible gene of schizophrenia. (PMID:24416398)
- The Gene-based analyses revealed four significant associations in the WT1, ZC3H12C, DLGAP2, and GPR1 genes at p < 0.05. in this study. (PMID:25391383)
- Results show that RP11-397D12.4, AC007403.1, and ERICH1-AS1 LncRNA expression are up-regulated in non-small-cell lung cancer (NSCLC) and may be potential biomarkers for predicting the tumorigenesis of NSCLC in the future. (PMID:26393913)
- This study showed increased DNA methylation levels of the DLGAP2 gene in both TD and NTD patients compared to control individuals. (PMID:30504779)
- Cannabis use is associated with potentially heritable widespread changes in autism candidate gene DLGAP2 DNA methylation in sperm. (PMID:31451081)
- Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer’s Dementia. (PMID:32877673)
- DNA Methylation Near DLGAP2 May Mediate the Relationship between Family History of Type 1 Diabetes and Type 1 Diabetes Risk. (PMID:38765731)
Cross-species orthologs
5 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | dlgap2a | ENSDARG00000059340 |
| danio_rerio | DLGAP2 | ENSDARG00000076070 |
| danio_rerio | dlgap2b | ENSDARG00000092376 |
| mus_musculus | Dlgap2 | ENSMUSG00000047495 |
| rattus_norvegicus | Dlgap2 | ENSRNOG00000012573 |
Paralogs (4): DLGAP4 (ENSG00000080845), DLGAP3 (ENSG00000116544), DLGAP5 (ENSG00000126787), DLGAP1 (ENSG00000170579)
Protein
Protein identifiers
Disks large-associated protein 2 — Q9P1A6 (reviewed: Q9P1A6)
Alternative names: PSD-95/SAP90-binding protein 2, SAP90/PSD-95-associated protein 2
All UniProt accessions (6): A0A0J9YWL8, A0A0J9YY16, A0A1B0GTN4, A0A1B0GXK6, Q9P1A6, H0YBY6
UniProt curated annotations — full annotation on UniProt →
Function. May play a role in the molecular organization of synapses and neuronal cell signaling. Could be an adapter protein linking ion channel to the subsynaptic cytoskeleton. May induce enrichment of PSD-95/SAP90 at the plasma membrane.
Subunit / interactions. Interacts with DLG1 and DLG4/PSD-95.
Subcellular location. Cell membrane. Postsynaptic density. Synapse.
Tissue specificity. Expressed in brain and kidney.
Similarity. Belongs to the SAPAP family.
Isoforms (3)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q9P1A6-1 | 1 | yes |
| Q9P1A6-2 | 2 | |
| Q9P1A6-3 | 3 |
RefSeq proteins (1): NP_001333739* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR005026 | SAPAP | Family |
Pfam: PF03359
UniProt features (32 total): modified residue 14, region of interest 6, compositionally biased region 6, splice variant 2, sequence variant 2, chain 1, sequence conflict 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9P1A6-F1 | 48.83 | 0.10 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Post-translational modifications (14): 298, 304, 386, 452, 662, 665, 668, 715, 738, 740, 771, 806, 978, 1007
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-6794361 | Neurexins and neuroligins |
MSigDB gene sets: 87 (showing top):
AAGCCAT_MIR135A_MIR135B, ATGCAGT_MIR217, CTATGCA_MIR153, GOBP_CELL_CELL_SIGNALING, GOBP_NEURON_NEURON_SYNAPTIC_TRANSMISSION, GOBP_SYNAPTIC_SIGNALING, CCCAGAG_MIR326, MODULE_207, MODULE_95, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, GOCC_POSTSYNAPSE, GOCC_SYNAPSE, GOCC_INTERMEDIATE_FILAMENT_CYTOSKELETON, BLALOCK_ALZHEIMERS_DISEASE_DN, GCACTTT_MIR175P_MIR20A_MIR106A_MIR106B_MIR20B_MIR519D
GO Biological Process (3): neuron-neuron synaptic transmission (GO:0007270), modulation of chemical synaptic transmission (GO:0050804), signaling (GO:0023052)
GO Molecular Function (2): molecular adaptor activity (GO:0060090), protein binding (GO:0005515)
GO Cellular Component (7): neurofilament (GO:0005883), plasma membrane (GO:0005886), postsynaptic density (GO:0014069), glutamatergic synapse (GO:0098978), postsynaptic specialization (GO:0099572), membrane (GO:0016020), synapse (GO:0045202)
Reactome top-level categories
Rollup of top-1 pathways:
| Category | Pathways |
|---|---|
| Protein-protein interactions at synapses | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| chemical synaptic transmission | 2 |
| binding | 2 |
| regulation of trans-synaptic signaling | 1 |
| regulation of biological process | 1 |
| molecular_function | 1 |
| cytoplasm | 1 |
| intermediate filament | 1 |
| membrane | 1 |
| cell periphery | 1 |
| asymmetric synapse | 1 |
| postsynaptic specialization | 1 |
| synapse | 1 |
| organelle | 1 |
| postsynapse | 1 |
| cellular anatomical structure | 1 |
| cell junction | 1 |
Protein interactions and networks
STRING
2126 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| DLGAP2 | SHANK2 | Q9UPX8 | 915 |
| DLGAP2 | SHANK3 | Q9BYB0 | 846 |
| DLGAP2 | PTCHD1 | Q96NR3 | 842 |
| DLGAP2 | SYNGAP1 | Q96PV0 | 818 |
| DLGAP2 | DDX53 | Q86TM3 | 694 |
| DLGAP2 | DLG4 | P78352 | 662 |
| DLGAP2 | NLGN4X | Q8N0W4 | 661 |
| DLGAP2 | NLGN3 | Q9NZ94 | 648 |
| DLGAP2 | ASTN2 | O75129 | 648 |
| DLGAP2 | NLGN1 | Q8N2Q7 | 601 |
| DLGAP2 | VLDLR | P98155 | 596 |
| DLGAP2 | KCNA4 | P22459 | 588 |
| DLGAP2 | CNTN4 | Q8IWV2 | 564 |
| DLGAP2 | CDH9 | Q9ULB4 | 563 |
| DLGAP2 | NRXN1 | Q9ULB1 | 531 |
IntAct
20 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| DLGAP2 | KRT40 | psi-mi:“MI:0915”(physical association) | 0.670 |
| KRT40 | DLGAP2 | psi-mi:“MI:0915”(physical association) | 0.670 |
| DLGAP2 | KRTAP4-2 | psi-mi:“MI:0915”(physical association) | 0.560 |
| KRTAP4-2 | DLGAP2 | psi-mi:“MI:0915”(physical association) | 0.560 |
| DLGAP2 | ABL1 | psi-mi:“MI:0915”(physical association) | 0.400 |
| DLGAP2 | CRK | psi-mi:“MI:0915”(physical association) | 0.400 |
| SRC | DLGAP2 | psi-mi:“MI:0915”(physical association) | 0.400 |
| FYN | DLGAP2 | psi-mi:“MI:0915”(physical association) | 0.400 |
| DLGAP2 | GRB2 | psi-mi:“MI:0915”(physical association) | 0.400 |
| DLGAP2 | NCK1 | psi-mi:“MI:0915”(physical association) | 0.400 |
| PIK3R1 | DLGAP2 | psi-mi:“MI:0915”(physical association) | 0.400 |
| DLGAP2 | SHANK3 | psi-mi:“MI:0915”(physical association) | 0.370 |
BioGRID (25): KRTAP4-2 (Two-hybrid), KRT40 (Two-hybrid), KRT40 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLG4 (Reconstituted Complex), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLGAP2 (Two-hybrid), DLG1 (Affinity Capture-MS)
ESM2 similar proteins: A0A1L8ER70, A1L253, A2AHC3, A5WUN7, B1AZP2, D4AEC2, O14490, P28290, P62024, P97836, P97839, Q148W8, Q14CH0, Q2KI52, Q2M3X8, Q3ZBW7, Q4KM62, Q4R2Y2, Q4R707, Q52KF3, Q5PQL8, Q5R3Z9, Q5RD34, Q5RJX2, Q5VUB5, Q5VZP5, Q5XII9, Q6GLU8, Q6NSV7, Q6P995, Q6PEI3, Q6RFY2, Q7T3E8, Q8BJ42, Q8BYK5, Q8C1B1, Q922B9, Q95X94, Q96BN6, Q96KR7
Diamond homologs: B1AZP2, O14490, O95886, P97836, P97837, P97838, P97839, Q15398, Q6PFD5, Q7K3L1, Q7ZYZ6, Q8BJ42, Q8K4R9, Q9D415, Q9P1A6, Q9Y2H0
SIGNOR signaling
4 interactions.
| A | Effect | B | Mechanism |
|---|---|---|---|
| DLGAP2 | “up-regulates activity” | DLG4 | binding |
| DLGAP2 | “up-regulates activity” | SHANK1 | relocalization |
| DLGAP2 | “up-regulates activity” | SHANK2 | relocalization |
| DLGAP2 | “up-regulates activity” | SHANK3 | relocalization |
Enriched among interaction partners
Reactome pathways and GO biological processes over-represented among this gene’s 10 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.
GO biological processes:
| GO term | Partners | Fold | FDR |
|---|---|---|---|
| ephrin receptor signaling pathway | 5 | 172.0× | 1e-08 |
Disease & clinical
Clinical variants and AI predictions
ClinVar
260 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 4 |
| Likely pathogenic | 1 |
| Uncertain significance | 205 |
| Likely benign | 27 |
| Benign | 11 |
Top pathogenic / likely-pathogenic (5)
| Variant ID | HGVS | Classification |
|---|---|---|
| 2685280 | GRCh37/hg19 8p23.3-23.1(chr8:158049-8093066)x1 | Pathogenic |
| 563521 | GRCh37/hg19 8p23.3(chr8:158048-1554662)x1 | Pathogenic |
| 57012 | GRCh38/hg38 8p23.3(chr8:241530-764384)x1 | Pathogenic |
| 57311 | GRCh38/hg38 8p23.3(chr8:241530-1371695)x1 | Pathogenic |
| 545353 | NC_000008.11:g.(?1050516)(1327901_?)del | Likely pathogenic |
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000001731 (8:1161546 C>G), RS1000003675 (8:910576 T>C), RS1000005061 (8:1620883 C>G), RS1000005934 (8:1648274 C>G), RS1000005990 (8:740480 C>G,T), RS1000007201 (8:1146555 GTGTGTGTGCACATGTGTGTGTATGCACA>G,GTGTGTGTGCACATGTGTGTGTATGCACATGTGTGTGCACATGTGTGTGTATGCACA), RS1000007513 (8:1522425 C>A,G), RS1000010423 (8:1686916 C>T), RS1000012305 (8:1024732 G>A), RS1000014835 (8:1380305 C>T), RS1000015633 (8:999129 A>G), RS1000015898 (8:1516371 G>A), RS1000015987 (8:1640699 T>C), RS1000018159 (8:1688229 C>T), RS1000021293 (8:970657 G>A)
Disease associations
OMIM: gene MIM:605438 | disease phenotypes: MIM:181500
GenCC curated gene-disease
ClinGen Gene-Disease Validity (1)
Expert-panel classifications — Definitive > Strong > Moderate > Limited > Disputed > Refuted.
| Disease | Classification | Inheritance |
|---|---|---|
| complex neurodevelopmental disorder | Limited | AD |
Mondo (1): schizophrenia (MONDO:0005090)
Orphanet (1): NON RARE IN EUROPE: Schizophrenia (Orphanet:3140)
HPO phenotypes
1 total (1 of 1 shown, HPO-id order):
| HPO | Term |
|---|---|
| HP:0100753 | Schizophrenia |
GWAS associations
20 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST001973_8 | Menarche (age at onset) | 6.000000e-07 |
| GCST002468_2 | Triglycerides | 7.000000e-09 |
| GCST002777_5 | Clozapine-induced cytotoxicity | 6.000000e-06 |
| GCST003264_93 | Post bronchodilator FEV1/FVC ratio | 2.000000e-06 |
| GCST003264_936 | Post bronchodilator FEV1/FVC ratio | 5.000000e-06 |
| GCST004748_129 | Lung cancer | 7.000000e-06 |
| GCST004992_1 | White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) | 6.000000e-07 |
| GCST006105_3 | Eye morphology | 8.000000e-08 |
| GCST006814_3 | End-stage renal disease | 1.000000e-06 |
| GCST006943_44 | Feeling miserable | 2.000000e-08 |
| GCST007160_18 | Refractive astigmatism | 4.000000e-06 |
| GCST008103_140 | Bipolar disorder | 3.000000e-06 |
| GCST008360_2 | Response to cognitive-behavioural therapy in anxiety disorder | 4.000000e-06 |
| GCST008513_16 | Health literacy | 9.000000e-06 |
| GCST008829_10 | Neuritic plaque | 9.000000e-06 |
| GCST011176_12 | Stroke | 4.000000e-07 |
| GCST011494_39 | Daytime nap | 3.000000e-13 |
| GCST011624_9 | Tau burden | 7.000000e-07 |
| GCST012490_269 | Femur bone mineral density x serum urate levels interaction | 2.000000e-09 |
| GCST012490_32 | Femur bone mineral density x serum urate levels interaction | 2.000000e-12 |
EFO canonical traits (12, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0004703 | age at menarche |
| EFO:0004530 | triglyceride measurement |
| EFO:0006952 | cytotoxicity measurement |
| EFO:0004713 | FEV/FVC ratio |
| EFO:0005674 | white matter microstructure measurement |
| EFO:0009598 | feeling miserable measurement |
| EFO:0007820 | cognitive behavioural therapy |
| EFO:0010104 | health literacy measurement |
| EFO:0006798 | neuritic plaque measurement |
| EFO:0007828 | daytime rest measurement |
| EFO:0004760 | t-tau measurement |
| EFO:0004531 | urate measurement |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
25 total (human), top 25 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| sodium arsenite | affects methylation, increases expression | 3 |
| Benzo(a)pyrene | affects methylation, decreases expression | 3 |
| bisphenol A | affects methylation, affects cotreatment, decreases methylation | 1 |
| testosterone undecanoate | increases expression, affects cotreatment | 1 |
| trichostatin A | decreases expression | 1 |
| 11-nor-delta(9)-tetrahydrocannabinol-9-carboxylic acid | affects methylation, increases abundance | 1 |
| benzo(e)pyrene | affects methylation | 1 |
| aflatoxin B2 | affects methylation | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| bisphenol S | decreases methylation | 1 |
| Resveratrol | affects cotreatment, decreases expression | 1 |
| Fulvestrant | affects cotreatment, decreases methylation | 1 |
| Acetaminophen | decreases expression | 1 |
| Air Pollutants | affects methylation, increases abundance | 1 |
| Arsenic | affects methylation | 1 |
| Cannabinoids | affects methylation, increases abundance | 1 |
| Copper | affects cotreatment, decreases expression | 1 |
| Cotinine | affects methylation, increases abundance | 1 |
| Methapyrilene | affects methylation | 1 |
| N-Nitrosopyrrolidine | decreases expression | 1 |
| Tobacco Smoke Pollution | affects methylation, increases abundance | 1 |
| Aflatoxin B1 | affects methylation | 1 |
| Levonorgestrel | affects cotreatment, increases expression | 1 |
| Sodium Selenite | decreases expression | 1 |
| Particulate Matter | affects methylation, increases abundance | 1 |
Clinical trials (associated diseases)
300 trials via MONDO — disease-level, not drug-specific.
| Trial | Phase | Status | Title |
|---|---|---|---|
| NCT00000374 | PHASE4 | COMPLETED | Treatment for First-Episode Schizophrenia |
| NCT00001656 | PHASE4 | COMPLETED | Comparison of Clozapine vs Olanzapine in Childhood-Onset Psychotic Disorders |
| NCT00007774 | PHASE4 | COMPLETED | To Determine if Olanzapine is More Cost Effective Than Haloperidol for the Treatment of Schizophrenia |
| NCT00014001 | PHASE4 | COMPLETED | CATIE- Schizophrenia Trial |
| NCT00018668 | PHASE4 | COMPLETED | Antipsychotic Response in Schizophrenia |
| NCT00034801 | PHASE4 | COMPLETED | Olanzapine Versus Active Comparator in the Treatment of Depression in Patients With Schizophrenia |
| NCT00034905 | PHASE4 | COMPLETED | A Comparison of Seroquel vs. Risperidone in Schizophrenia |
| NCT00036088 | PHASE4 | COMPLETED | Olanzapine Versus An Active Comparator in the Treatment of Schizophrenia |
| NCT00044187 | PHASE4 | COMPLETED | The Assessment of a Weight-Gain Agent for the Treatment of Olanzapine-Associated Anti-Obesity Agent in Patients With Schizophrenia, Schizophreniform Disorder, Schizoaffective Disorder, and Bipolar I Disorder |
| NCT00044655 | PHASE4 | COMPLETED | Switching Medication to Treat Schizophrenia |
| NCT00048828 | PHASE4 | COMPLETED | Treating Drug-Resistant Childhood Schizophrenia |
| NCT00053703 | PHASE4 | COMPLETED | Treatment of Early Onset Schizophrenia Spectrum Disorders (TEOSS) |
| NCT00056498 | PHASE4 | COMPLETED | Risperidone Treatment in Schizophrenia Patients Who Are Currently Taking Clozapine |
| NCT00061802 | PHASE4 | COMPLETED | Efficacy and Safety of Two Atypical Antipsychotics vs. Placebo in Patients With an Acute Exacerbation of Either Schizophrenia or Schizoaffective Disorder |
| NCT00080327 | PHASE4 | COMPLETED | Study of Three Doses of Aripiprazole in Patients With Acute Schizophrenia |
| NCT00088049 | PHASE4 | COMPLETED | Study of Olanzapine vs. Aripiprazole in the Treatment of Schizophrenia |
| NCT00090012 | PHASE4 | COMPLETED | Comparison of Continuing Olanzapine to Switching to Quetiapine in Overweight or Obese Patients With Schizophrenia and Schizoaffective Disorder |
| NCT00100776 | PHASE4 | COMPLETED | Efficacy of High Dose Olanzapine for the Treatment of Schizophrenia and Schizoaffective Disorder |
| NCT00103571 | PHASE4 | COMPLETED | Olanzapine Versus Aripiprazole in the Treatment of Acutely Ill Patients With Schizophrenia |
| NCT00108368 | PHASE4 | COMPLETED | The Effects of Risperidone and Olanzapine on Thinking |
| NCT00114595 | PHASE4 | COMPLETED | Ethyl-Eicosapentaenoic Acid and Tardive Dyskinesia |
| NCT00130923 | PHASE4 | COMPLETED | Risperidone Long-acting Versus Oral Risperidone in Patients With Schizophrenia and Alcohol Use Disorder |
| NCT00137020 | PHASE4 | COMPLETED | Clinical Effect Of Cross Titration Of Antipsychotics With Ziprasidone In Schizophrenia Or Schizoaffective Disorder |
| NCT00140166 | PHASE4 | COMPLETED | Treatment of Acute Schizophrenia With Vitamin Therapy |
| NCT00145847 | PHASE4 | COMPLETED | Naltrexone Treatment of Alcohol Abuse in Schizophrenia |
| NCT00148564 | PHASE4 | COMPLETED | Energy Homeostasis Under Treatment With Atypical Antipsychotics |
| NCT00156715 | PHASE4 | COMPLETED | Efficacy of Quetiapine in the Treatment of Patients With Schizophrenia and a Comorbid Substance Use Disorder |
| NCT00158223 | PHASE4 | COMPLETED | Effectiveness of Pimozide in Augmenting the Effects of Clozapine in the Treatment of Schizophrenia |
| NCT00159081 | PHASE4 | COMPLETED | One Year Drug Treatment in First-Episode Schizophrenia |
| NCT00159120 | PHASE4 | COMPLETED | Maintenance Treatment vs. Stepwise Drug Discontinuation in First-Episode Schizophrenia |
| NCT00159133 | PHASE4 | COMPLETED | Prodrome-Based Early Intervention With Antipsychotics vs. Benzodiazepines in First-Episode Schizophrenia |
| NCT00159757 | PHASE4 | TERMINATED | 12 Week Open, Non-Comparative Switch Study Of Oral Ziprazidone In Previously Treated Schizophrenic Patients |
| NCT00167817 | PHASE4 | COMPLETED | Effect of Switch to Aripiprazole on Health and Smoking Parameters in Patients With Schizophrenia: A Pilot Study |
| NCT00169026 | PHASE4 | TERMINATED | Alcoholism and Schizophrenia: Effects of Clozapine |
| NCT00169039 | PHASE4 | TERMINATED | Clozapine Versus Chlorpromazine for Treatment-Unresponsive Schizophrenia |
| NCT00169065 | PHASE4 | COMPLETED | Effectiveness of Clozapine Versus Olanzapine for Treatment-resistant Schizophrenia |
| NCT00169091 | PHASE4 | TERMINATED | Clozapine Versus Haloperidol for Treating the First Episode of Schizophrenia |
| NCT00176423 | PHASE4 | COMPLETED | Efficacy Study of Galantamine for Cognitive Impairments in Schizophrenia |
| NCT00176436 | PHASE4 | COMPLETED | Atomoxetine for Treatment of Weight Gain in Olanzapine or Clozapine Patients |
| NCT00177008 | PHASE4 | COMPLETED | Aripiprazole for the Treatment of Schizophrenia With Co-Morbid Social Anxiety |
Related Atlas pages
- Associated diseases: complex neurodevelopmental disorder