TVP23C

gene
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Also known as MGC8763

Summary

TVP23C (trans-golgi network vesicle protein 23 homolog C, HGNC:30453) is a protein-coding gene on chromosome 17p12, encoding Golgi apparatus membrane protein TVP23 homolog C (Q96ET8).

Predicted to be involved in protein secretion and vesicle-mediated transport. Predicted to be located in membrane. Predicted to be active in Golgi membrane.

Source: NCBI Gene 201158 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 6 total — 2 pathogenic
  • MANE Select transcript: NM_001135036

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:30453
Approved symbolTVP23C
Nametrans-golgi network vesicle protein 23 homolog C
Location17p12
Locus typegene with protein product
StatusApproved
AliasesMGC8763
Ensembl geneENSG00000175106
Ensembl biotypeprotein_coding
Entrez201158

Gene structure

Transcript identifiers

Ensembl transcripts: 10 — 6 protein_coding, 3 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000225576, ENST00000419890, ENST00000428082, ENST00000438826, ENST00000518321, ENST00000521179, ENST00000523573, ENST00000581273, ENST00000583206, ENST00000584811

RefSeq mRNA: 2 — MANE Select: NM_001135036 NM_001135036, NM_145301

CCDS: CCDS11170, CCDS45617

Canonical transcript exons

ENST00000518321 — 6 exons

ExonStartEnd
ENSE000021379981556343715563483
ENSE000027154201553698015540561
ENSE000034627851555368515553829
ENSE000035490541554578515545916
ENSE000036063801555528215555364
ENSE000036792661554705915547148

Expression profiles

Bgee: expression breadth ubiquitous, 168 present calls, max score 96.18.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0076 / max 1.9397, expressed in 1 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1646910.9396567
1646920.00761

Top tissues by expression

229 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548896.18gold quality
colonic epitheliumUBERON:000039791.83gold quality
bone marrow cellCL:000209290.04gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047389.28gold quality
calcaneal tendonUBERON:000370186.13gold quality
adrenal tissueUBERON:001830386.05gold quality
lower esophagus mucosaUBERON:003583484.01gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099183.10gold quality
adenohypophysisUBERON:000219682.96gold quality
left ovaryUBERON:000211981.59gold quality
islet of LangerhansUBERON:000000681.51gold quality
stromal cell of endometriumCL:000225580.91gold quality
pituitary glandUBERON:000000780.82gold quality
right uterine tubeUBERON:000130280.32gold quality
right ovaryUBERON:000211880.15gold quality
left lobe of thyroid glandUBERON:000112080.11gold quality
right lobe of thyroid glandUBERON:000111979.58gold quality
thyroid glandUBERON:000204679.26gold quality
ectocervixUBERON:001224979.25gold quality
endocervixUBERON:000045879.15gold quality
left adrenal gland cortexUBERON:003582579.13gold quality
body of uterusUBERON:000985379.05gold quality
uterine cervixUBERON:000000278.84gold quality
descending thoracic aortaUBERON:000234578.82gold quality
olfactory segment of nasal mucosaUBERON:000538678.80gold quality
ascending aortaUBERON:000149678.75gold quality
popliteal arteryUBERON:000225078.67gold quality
tibial arteryUBERON:000761078.67gold quality
thoracic aortaUBERON:000151578.62gold quality
ganglionic eminenceUBERON:000402378.53gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes6.21

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

22 targeting TVP23C, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-7110-3P100.0073.182486
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-6845-3P99.9466.881439
HSA-MIR-368699.9070.532432
HSA-MIR-6817-3P99.7968.352126
HSA-MIR-57799.7869.132479
HSA-MIR-129999.7771.242389
HSA-MIR-6887-3P99.6667.831778
HSA-MIR-427999.1966.702437
HSA-MIR-7109-5P99.1866.131057
HSA-MIR-4758-3P99.1263.96869
HSA-MIR-328-5P99.0864.651000
HSA-MIR-6885-5P98.7164.33902
HSA-MIR-6804-5P98.3965.771084
HSA-MIR-6826-3P98.1966.321153
HSA-MIR-7111-3P97.8066.751467
HSA-MIR-4723-3P97.6765.911017
HSA-MIR-6769B-3P97.4165.531036
HSA-MIR-318397.4065.68978
HSA-MIR-10401-3P91.6666.0197

Cross-species orthologs

7 orthologs

OrganismSymbolGene ID
danio_reriozgc:112148ENSDARG00000001804
danio_reriotvp23bENSDARG00000057060
mus_musculusTvp23bENSMUSG00000014177
rattus_norvegicusAABR07006081.1ENSRNOG00000016597
rattus_norvegicusTvp23bENSRNOG00000050649
drosophila_melanogasterCG5021FBGN0035944
caenorhabditis_elegansWBGENE00016400

Paralogs (2): TVP23A (ENSG00000166676), TVP23B (ENSG00000171928)

Protein

Protein identifiers

Golgi apparatus membrane protein TVP23 homolog CQ96ET8 (reviewed: Q96ET8)

All UniProt accessions (7): C9JPH1, C9JYS5, E5RGC5, E5RIS5, J3QL47, K7EK95, Q96ET8

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the TVP23 family.

Isoforms (3)

UniProt IDNamesCanonical?
Q96ET8-11yes
Q96ET8-22
Q96ET8-33

RefSeq proteins (2): NP_001128508, NP_660344 (=MANE)

Domains & families (InterPro)

IDNameType
IPR008564TVP23-likeFamily

Pfam: PF05832

UniProt features (16 total): sequence conflict 4, splice variant 4, transmembrane region 2, sequence variant 2, region of interest 2, chain 1, modified residue 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96ET8-F159.620.02

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 (1): 1

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 67 (showing top): chr17p12, GOBP_VESICLE_MEDIATED_TRANSPORT, GOBP_SECRETION, GRYDER_PAX3FOXO1_ENHANCERS_IN_TADS, FORTSCHEGGER_PHF8_TARGETS_DN, HMG20B_TARGET_GENES, NAB2_TARGET_GENES, MIR616_5P, MIR371B_5P, MIR373_5P, MIR548AJ_3P_MIR548X_3P, MIR548AE_3P_MIR548AQ_3P, MIR548AH_3P_MIR548AM_3P, MIR548J_3P, MIR3658

GO Biological Process (2): protein secretion (GO:0009306), vesicle-mediated transport (GO:0016192)

GO Molecular Function (0):

GO Cellular Component (2): Golgi membrane (GO:0000139), membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein transport1
secretion by cell1
establishment of protein localization to extracellular region1
protein localization to extracellular region1
transport1
cellular process1
Golgi apparatus1
bounding membrane of organelle1
cellular anatomical structure1

Protein interactions and networks

STRING

366 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TVP23CCDRT4Q8N9R6728
TVP23CCDRT15Q96T59579
TVP23CCCDC182A6NF36507
TVP23CUBAP1LF5GYI3479
TVP23CSMCO2A6NFE2447
TVP23CTEKT3Q9BXF9418
TVP23CRGPD1P0C839398
TVP23CCFAP157Q5JU67396
TVP23CTRMT13Q9NUP7378
TVP23CMS4A14Q96JA4375
TVP23CUEVLDQ8IX04370
TVP23CKLHL28Q9NXS3370
TVP23CANKRD33BA6NCL7354
TVP23CCEP95Q96GE4354
TVP23CSREK1IP1Q8N9Q2349

IntAct

59 interactions, top by confidence:

ABTypeScore
RINT1NBASpsi-mi:“MI:0914”(association)0.830
RANBP6SLC27A2psi-mi:“MI:0914”(association)0.640
BZW2ENDOD1psi-mi:“MI:0914”(association)0.640
TMEM9ESYT2psi-mi:“MI:0914”(association)0.530
TOR1AIP2TMEM223psi-mi:“MI:0914”(association)0.530
SLC7A1TMEM223psi-mi:“MI:0914”(association)0.530
HTR2CKLRG2psi-mi:“MI:0914”(association)0.530
VSIG4TCAF2psi-mi:“MI:0914”(association)0.530
SLC15A1METTL15psi-mi:“MI:0914”(association)0.530
IL13RA2METTL15psi-mi:“MI:0914”(association)0.530
SLC2A12METTL15psi-mi:“MI:0914”(association)0.530
TPCN2AP3B1psi-mi:“MI:0914”(association)0.530
TSPAN5SC5Dpsi-mi:“MI:0914”(association)0.530
ALOX5DDHD2psi-mi:“MI:0914”(association)0.530
FUCA2HSPA5psi-mi:“MI:0914”(association)0.530
TMEM63AAP3D1psi-mi:“MI:0914”(association)0.530
TMEM223psi-mi:“MI:0914”(association)0.350
TTYH1TMEM223psi-mi:“MI:0914”(association)0.350
TSPAN15TMEM223psi-mi:“MI:0914”(association)0.350
SLC7A14TMEM120Bpsi-mi:“MI:0914”(association)0.350
GPR17TMEM120Bpsi-mi:“MI:0914”(association)0.350
LRRC55TMEM120Bpsi-mi:“MI:0914”(association)0.350
ATP2A1TMEM120Bpsi-mi:“MI:0914”(association)0.350
C5AR1TCAF2psi-mi:“MI:0914”(association)0.350
GPR182METTL15psi-mi:“MI:0914”(association)0.350
SLC22A4RTL8Cpsi-mi:“MI:0914”(association)0.350
AQP3RTL8Cpsi-mi:“MI:0914”(association)0.350
EDEM2HACD1psi-mi:“MI:0914”(association)0.350

BioGRID (75): TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-MS), TVP23C (Affinity Capture-RNA)

ESM2 similar proteins: A4Q9F3, A8IHN8, D3YYI7, M0R7T9, O09112, O60347, O88751, P51509, Q09YL6, Q0IHH1, Q13202, Q13505, Q14190, Q147X3, Q17QD9, Q3TZ87, Q3UPL5, Q3V1H9, Q5TGI4, Q5VUJ9, Q5VV17, Q5XI57, Q61079, Q6A039, Q6PDS0, Q6ZVT0, Q7Z7K6, Q80UW0, Q86YJ5, Q8C4U2, Q8CES0, Q8N554, Q8N8J7, Q8TC41, Q8TDR2, Q8WWW0, Q96AQ8, Q96ET8, Q96KN8, Q96MM7

Diamond homologs: A1CIM7, A1CW41, A2Q9P5, A3LRT4, A4RME3, A5DRE8, A6NH52, A6SFL7, A6ZY50, A7TGB4, A8N1Z1, B0CQN9, B0Y4Q8, B2ALT5, P38962, Q0CSZ7, Q0UV43, Q18449, Q1E9X9, Q29S14, Q2UUK2, Q4WQJ5, Q54LC9, Q5APA2, Q5R9I4, Q6BVH1, Q6C7V5, Q6CTK9, Q6FM91, Q74ZP5, Q7SGB6, Q8IQC1, Q8LEK2, Q96ET8, Q9D8T4, Q9NYZ1, Q9Y7K7, Q86I95, O14628, O94966

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 86 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 termPartnersFoldFDR
transport across blood-brain barrier613.6×3e-03

Disease & clinical

Clinical variants and AI predictions

ClinVar

6 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic2
Likely pathogenic0
Uncertain significance1
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (2)

Variant IDHGVSClassification
1808684GRCh37/hg19 17p12(chr17:14087934-15491532)x1Pathogenic
523259GRCh37/hg19 17p12(chr17:14215739-15422582)Pathogenic

SpliceAI

1513 predictions. Top by Δscore:

VariantEffectΔscore
17:15540432:CTTGT:Cdonor_gain1.0000
17:15545777:ATACT:Adonor_loss1.0000
17:15545779:AC:Adonor_loss1.0000
17:15545780:CTCA:Cdonor_loss1.0000
17:15545781:TCAC:Tdonor_loss1.0000
17:15545782:C:CGdonor_loss1.0000
17:15545782:CACCA:Cdonor_loss1.0000
17:15545783:A:ACdonor_gain1.0000
17:15545783:A:Tdonor_loss1.0000
17:15545783:ACCAG:Adonor_gain1.0000
17:15545784:C:Adonor_loss1.0000
17:15545784:C:CCdonor_gain1.0000
17:15545784:CCAGC:Cdonor_gain1.0000
17:15545828:A:ACdonor_gain1.0000
17:15545914:CTC:Cacceptor_gain1.0000
17:15545915:TC:Tacceptor_gain1.0000
17:15545916:CC:Cacceptor_gain1.0000
17:15545916:CCT:Cacceptor_loss1.0000
17:15545916:CCTA:Cacceptor_loss1.0000
17:15545917:C:Aacceptor_loss1.0000
17:15545917:C:CCacceptor_gain1.0000
17:15545918:T:Cacceptor_loss1.0000
17:15545918:T:Gacceptor_loss1.0000
17:15547053:CTTTA:Cdonor_loss1.0000
17:15547054:TTTA:Tdonor_loss1.0000
17:15547055:TTA:Tdonor_loss1.0000
17:15547055:TTACC:Tdonor_loss1.0000
17:15547056:TACC:Tdonor_loss1.0000
17:15547058:CC:Cdonor_loss1.0000
17:15547058:CCT:Cdonor_loss1.0000

AlphaMissense

1344 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
17:15545866:A:CF127L0.972
17:15545866:A:TF127L0.972
17:15545868:A:GF127L0.972
17:15547071:A:CF106L0.971
17:15547071:A:TF106L0.971
17:15547073:A:GF106L0.971
17:15553685:C:AK80N0.969
17:15553685:C:GK80N0.969
17:15547115:A:GW92R0.966
17:15547115:A:TW92R0.966
17:15553787:A:CS46R0.964
17:15553787:A:TS46R0.964
17:15553789:T:GS46R0.964
17:15553697:A:CF76L0.963
17:15553697:A:TF76L0.963
17:15553699:A:GF76L0.963
17:15547077:C:AW104C0.944
17:15547077:C:GW104C0.944
17:15547146:A:CN81K0.944
17:15547146:A:TN81K0.944
17:15547079:A:GW104R0.938
17:15547079:A:TW104R0.938
17:15553700:G:CD75E0.936
17:15553700:G:TD75E0.936
17:15547110:C:AW93C0.933
17:15547110:C:GW93C0.933
17:15553701:T:AD75V0.930
17:15553796:A:CF43L0.929
17:15553796:A:TF43L0.929
17:15553798:A:GF43L0.929

dbSNP variants (sampled 300 via entrez): RS1000026878 (17:15515760 T>A,C), RS1000028694 (17:15561426 C>G), RS1000168876 (17:15535640 C>A), RS1000198754 (17:15510028 G>A), RS1000275774 (17:15541720 T>C), RS1000304485 (17:15535173 T>C), RS1000323685 (17:15554052 T>C), RS1000371847 (17:15504690 T>C), RS1000387972 (17:15548446 T>C), RS1000471990 (17:15506032 A>G), RS1000501315 (17:15536955 G>T), RS1000557553 (17:15518255 G>A), RS1000652500 (17:15509547 T>C,G), RS1000664393 (17:15542694 C>G,T), RS1000694686 (17:15502350 T>C)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (2): myopathy (MONDO:0005336), attention deficit-hyperactivity disorder (MONDO:0007743)

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

29 total (human), top 29 by PubMed support.

ChemicalActions (top 5)PubMed papers
Tobacco Smoke Pollutiondecreases expression, increases expression2
bisphenol Faffects cotreatment, decreases expression1
sodium arseniteincreases expression1
benzo(e)pyreneincreases methylation1
ferrous chlorideincreases expression1
arsenic disulfideincreases methylation1
perfluorooctane sulfonic acidincreases expression1
CGP 52608affects binding, increases reaction1
K 7174increases expression1
abrineincreases expression1
Resveratrolaffects cotreatment, increases expression1
Sunitinibincreases expression1
Air Pollutantsincreases abundance, increases expression1
Arsenicalsdecreases expression1
Benzo(a)pyreneaffects methylation1
Cadmiumincreases abundance, increases expression1
Caffeinedecreases phosphorylation1
Dexamethasoneaffects cotreatment, decreases expression1
Indomethacindecreases expression, affects cotreatment1
Methapyrileneincreases methylation1
Plant Extractsaffects cotreatment, increases expression1
Tunicamycinincreases expression1
1-Methyl-3-isobutylxanthineaffects cotreatment, decreases expression1
Cyclosporineincreases expression1
Aflatoxin B1increases methylation1
Cadmium Chlorideincreases abundance, increases expression1
Thapsigarginincreases expression1
Okadaic Acidincreases expression1
Particulate Matterincreases abundance, increases expression1

Clinical trials (associated diseases)

300 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT00120055PHASE4COMPLETEDAssociation Between Systemic Exposure of Atorvastatin and Metabolites and Atorvastatin-induced Myotoxicity
NCT03633565PHASE4UNKNOWNComparative Study of Strategies for Management of Duchenne Myopathy (DM)
NCT00152750PHASE4UNKNOWNStudy of Clonidine on Sleep Architecture in Children With Tourette’s Syndrome (TS) and Comorbid ADHD
NCT00181571PHASE4COMPLETEDA Double-Blind Comparison of Concerta and Placebo in Adults With Attention Deficit Hyperactivity Disorder
NCT00181675PHASE4COMPLETEDA Double-Blind Comparison of Galantamine HBr and Placebo in Adults With Attention Deficit Hyperactivity Disorder
NCT00181714PHASE4COMPLETEDPrevention of Cigarette Smoking in Attention Deficit Hyperactivity Disorder (ADHD) Youth With Concerta
NCT00181948PHASE4COMPLETEDStrattera Treatment in Children With ADHD Who Have Poor Response to Stimulant Therapy
NCT00181987PHASE4COMPLETEDConcerta in the Treatment of ADHD in Youth and Adults With Bipolar Disorder
NCT00190736PHASE4COMPLETEDEfficacy and Safety of Once-Daily Atomoxetine Hydrochloride in Adults With ADHD Over an Extended Period of Time (6 Months)
NCT00190775PHASE4COMPLETEDA Randomized, Double-Blind Comparison of Placebo and Atomoxetine Hydrochloride Given Once a Day in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
NCT00190879PHASE4COMPLETEDPlacebo-Controlled Study of Atomoxetine Hydrochloride in the Treatment of Adults With ADHD and Comorbid Social Anxiety Disorder
NCT00190957PHASE4COMPLETEDAtomoxetine Treatment of Adults With ADHD and Comorbid Alcohol Abuse
NCT00191035PHASE4COMPLETEDMaintenance of Benefit With Atomoxetine Hydrochloride in Adolescents With ADHD
NCT00191048PHASE4COMPLETEDTreatment With Atomoxetine Hydrochloride in Children and Adolescents With ADHD
NCT00191633PHASE4COMPLETEDStudy of Atomoxetine in Children With ADHD to Assess Symptomatic and Functional Outcomes
NCT00191906PHASE4COMPLETEDComparison of Atomoxetine and Placebo in Children With Attention-Deficit/Hyperactivity Disorder (ADHD) and/or Reading Disorder (RD)
NCT00216918PHASE4COMPLETEDNeuropsychological Functioning in Children With Attention-Deficit/Hyperactivity Disorder.
NCT00221962PHASE4COMPLETEDStudy of Aripiprazole (Abilify) in Children With ADHD (Attention Deficit Hyperactivity Disorder)
NCT00223561PHASE4COMPLETEDMethylphenidate and Driving Ability in Adult Patients With Attention-Deficit Hyperactivity Disorder
NCT00299234PHASE4TERMINATEDAtomoxetine for Children With Acquired Attentional Disorders Following Completion of Chemotherapy for ALL
NCT00302406PHASE4COMPLETEDNaturalistic Substitution of Concerta in Adult Subject With ADHD Receiving Immediate Release Methylphenidate
NCT00305370PHASE4COMPLETEDAripiprazole Associated With Methylphenidate in Children and Adolescents With Bipolar Disorder and ADHD
NCT00381758PHASE4COMPLETEDThe COMACS Study: A Comparison of Methylphenidates in an Analog Classroom Setting
NCT00406354PHASE4COMPLETEDComparison of Atomoxetine Versus Placebo in Children and Adolescents With ADHD and Comorbid ODD in Germany
NCT00434213PHASE4COMPLETEDCharacterization of Dermal Reactions in Pediatric Patients With ADHD Using DAYTRANA
NCT00468143PHASE4COMPLETEDA Within-Subject Cross-Over Comparison Between Immediate Release and Extended Release Adderall
NCT00471354PHASE4COMPLETEDA Study for Patients With Attention-Deficit/Hyperactivity Disorder Treated With Atomoxetine
NCT00483106PHASE4COMPLETEDClinical and Pharmacogenetic Study of Attention Deficit With Hyperactivity Disorder (ADHD)
NCT00485849PHASE4COMPLETEDA Study of Atomoxetine for Attention Deficit and Hyperactive/Impulsive Behaviour Problems in Children With ASD
NCT00485875PHASE4COMPLETEDSafety and Efficacy of Switching From a Stimulant Medication to Atomoxetine in Children and Adolescents With ADHD
NCT00486122PHASE4COMPLETEDEvaluation of Continuous Symptom Treatment of ADHD
NCT00500071PHASE4COMPLETEDDose-Optimization Study Evaluating the Efficacy, Safety and Tolerability of Vyvanse (Lisdexamfetamine Dimesylate) in Children Aged 6-12 Diagnosed With ADHD
NCT00506727PHASE4COMPLETEDAnalog Classroom Study Comparison of ADDERALL XR With STRATTERA in Children Aged 6-12 With ADHD
NCT00510276PHASE4COMPLETEDTreatment of Attention-Deficit/Hyperactivity Disorder (ADHD) With Atomoxetine in Young Adults and Its Effects on Functional Outcomes
NCT00517504PHASE4COMPLETEDMethylphenidate Study in Young Children With Developmental Disorders
NCT00517647PHASE4COMPLETEDAtomoxetine Pilot Study in Preschool Children With ADHD
NCT00518232PHASE4COMPLETEDA Study to Determine Effective and Tolerable Titration Scheme for OROS-Methylphenidate in Children With Attention-deficit Hyperactivity Disorder
NCT00530257PHASE4COMPLETEDStudy of the Effects of Osmotic-Release Oral System (OROS) Methylphenidate (Concerta) on Attention and Memory
NCT00536419PHASE4UNKNOWNImpact of Attention Deficit/Hyperactivity Disorder and Substance Use Disorder on Motorcycle Traffic Accidents
NCT00546910PHASE4COMPLETEDComparison of Atomoxetine Versus Placebo in Children With Attention-Deficit/Hyperactivity Disorder (ADHD)
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): myopathy