ZNF37A

gene
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Also known as KOX21ZNF37

Summary

ZNF37A (zinc finger protein 37A, HGNC:13102) is a protein-coding gene on chromosome 10p11.1, encoding Zinc finger protein 37A (P17032). May be involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus.

Source: NCBI Gene 7587 — RefSeq curated summary.

At a glance

  • Gene–disease (curated): Tourette syndrome (No Known Disease Relationship, GenCC)
  • GWAS associations: 1
  • Clinical variants (ClinVar): 93 total
  • MANE Select transcript: NM_001324250

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:13102
Approved symbolZNF37A
Namezinc finger protein 37A
Location10p11.1
Locus typegene with protein product
StatusApproved
AliasesKOX21, ZNF37
Ensembl geneENSG00000075407
Ensembl biotypeprotein_coding
OMIM616085
Entrez7587

Gene structure

Transcript identifiers

Ensembl transcripts: 27 — 24 protein_coding, 3 protein_coding_CDS_not_defined

ENST00000351773, ENST00000361085, ENST00000477790, ENST00000479469, ENST00000498773, ENST00000638053, ENST00000685332, ENST00000865425, ENST00000865426, ENST00000865427, ENST00000865428, ENST00000865429, ENST00000865430, ENST00000865431, ENST00000865432, ENST00000865433, ENST00000865434, ENST00000865436, ENST00000865437, ENST00000865438, ENST00000865439, ENST00000865440, ENST00000865441, ENST00000950340, ENST00000950341, ENST00000950342, ENST00000950343

RefSeq mRNA: 20 — MANE Select: NM_001324250 NM_001007094, NM_001178101, NM_001324245, NM_001324246, NM_001324247, NM_001324248, NM_001324249, NM_001324250, NM_001324251, NM_001324252, NM_001324253, NM_001324254, NM_001324256, NM_001324257, NM_001324258, NM_001324259, NM_001324260, NM_001324261, NM_001324262, NM_003421

CCDS: CCDS31183, CCDS81451

Canonical transcript exons

ENST00000685332 — 8 exons

ExonStartEnd
ENSE000013937573809493138095224
ENSE000013944713809574438095804
ENSE000024865543811519538115290
ENSE000034937083809657438096632
ENSE000035106133811475538114881
ENSE000037995413809553838095629
ENSE000039250033811739038124625
ENSE000039307683809433738094490

Expression profiles

Bgee: expression breadth ubiquitous, 256 present calls, max score 96.24.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 8.6279 / max 95.3759, expressed in 1657 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1047228.62791657

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
parotid glandUBERON:000183196.24gold quality
visceral pleuraUBERON:000240195.34gold quality
parietal pleuraUBERON:000240094.32gold quality
tibiaUBERON:000097994.15gold quality
pleuraUBERON:000097793.11gold quality
buccal mucosa cellCL:000233691.23gold quality
tendon of biceps brachiiUBERON:000818890.27gold quality
seminal vesicleUBERON:000099890.19gold quality
deciduaUBERON:000245089.20gold quality
primary visual cortexUBERON:000243688.45gold quality
Brodmann (1909) area 23UBERON:001355488.13gold quality
tendonUBERON:000004387.67gold quality
cerebellar vermisUBERON:000472087.56gold quality
postcentral gyrusUBERON:000258187.03gold quality
calcaneal tendonUBERON:000370186.88gold quality
colonic epitheliumUBERON:000039786.29gold quality
corpus callosumUBERON:000233685.58gold quality
parietal lobeUBERON:000187285.57gold quality
sural nerveUBERON:001548885.55gold quality
medial globus pallidusUBERON:000247785.52gold quality
entorhinal cortexUBERON:000272885.31gold quality
occipital lobeUBERON:000202185.24gold quality
cerebellar cortexUBERON:000212984.96gold quality
cerebellar hemisphereUBERON:000224584.92gold quality
globus pallidusUBERON:000187584.61gold quality
right hemisphere of cerebellumUBERON:001489084.52gold quality
germinal epithelium of ovaryUBERON:000130484.27gold quality
cerebellumUBERON:000203784.00gold quality
superior frontal gyrusUBERON:000266183.90gold quality
pituitary glandUBERON:000000783.89gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes6.32

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

122 targeting ZNF37A, 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-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-6759-5P99.9966.54785
HSA-MIR-511-3P99.9968.851467
HSA-MIR-3692-3P99.9870.272139
HSA-MIR-477599.9875.006394
HSA-MIR-4482-3P99.9872.503147
HSA-MIR-6888-3P99.9765.951170
HSA-MIR-590-3P99.9674.346478
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-767-5P99.9570.85993
HSA-MIR-9983-3P99.9471.483631
HSA-MIR-218-5P99.9372.222103
HSA-MIR-539-5P99.9370.302855
HSA-MIR-335-3P99.9373.364958
HSA-MIR-6508-5P99.9270.672465
HSA-MIR-450B-5P99.9271.483175
HSA-MIR-6809-3P99.9171.453814
HSA-MIR-368699.9070.532432
HSA-MIR-95-5P99.8972.173973
HSA-MIR-129-5P99.8870.263273
HSA-MIR-806799.8669.592260
HSA-MIR-6515-3P99.8268.191933
HSA-MIR-3180-5P99.8269.122422
HSA-MIR-684499.8270.692423
HSA-MIR-4659A-3P99.8072.624248
HSA-MIR-4659B-3P99.8072.624248
HSA-MIR-4760-5P99.8069.881619
HSA-MIR-374C-5P99.8072.062910
HSA-MIR-655-3P99.8072.192909

Literature-anchored findings (GeneRIF, showing 2)

  • This suggests that the pathological molecular mechanisms linking ZNF37A and myogenesis may involve the signaling pathway that is known to promote myoblast recruitment during development and regeneration (PMID:23922231)
  • ZNF37A promotes tumor metastasis through transcriptional control of THSD4/TGF-beta axis in colorectal cancer. (PMID:33875786)

Cross-species orthologs

0 orthologs

Paralogs (176): ZNF195 (ENSG00000005801), ZNF112 (ENSG00000062370), ZNF275 (ENSG00000063587), ZNF510 (ENSG00000081386), ZNF506 (ENSG00000081665), ZNF268 (ENSG00000090612), MZF1 (ENSG00000099326), ZNF629 (ENSG00000102870), ZNF175 (ENSG00000105497), ZNF85 (ENSG00000105750), ZFP30 (ENSG00000120784), ZNF45 (ENSG00000124459), ZNF391 (ENSG00000124613), ZNF436 (ENSG00000125945), ZNF484 (ENSG00000127081), ZNF835 (ENSG00000127903), ZNF780B (ENSG00000128000), ZSCAN10 (ENSG00000130182), ZNF317 (ENSG00000130803), ZNF331 (ENSG00000130844), ZNF227 (ENSG00000131115), ZNF141 (ENSG00000131127), ZNF132 (ENSG00000131849), ZNF189 (ENSG00000136870), ZIM3 (ENSG00000141946), ZFP14 (ENSG00000142065), ZNF514 (ENSG00000144026), ZNF300 (ENSG00000145908), RBAK (ENSG00000146587), ZNF157 (ENSG00000147117), ZNF182 (ENSG00000147118), ZNF41 (ENSG00000147124), ZNF7 (ENSG00000147789), ZNF117 (ENSG00000152926), ZNF221 (ENSG00000159905), ZNF235 (ENSG00000159917), ZNF714 (ENSG00000160352), ZNF577 (ENSG00000161551), ZNF12 (ENSG00000164631), ZNF3 (ENSG00000166526)

Protein

Protein identifiers

Zinc finger protein 37AP17032 (reviewed: P17032)

Alternative names: Zinc finger protein KOX21

All UniProt accessions (2): P17032, A0A1B0GVV4

UniProt curated annotations — full annotation on UniProt →

Function. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Induction. Down-regulated in cells with DM1 (Myotonic dystrophy type 1) mutation, via a mechanism that involves abnormal control of its mRNA stability by CUGBP1.

Similarity. Belongs to the krueppel C2H2-type zinc-finger protein family.

RefSeq proteins (20): NP_001007095, NP_001171572, NP_001311174, NP_001311175, NP_001311176, NP_001311177, NP_001311178, NP_001311179, NP_001311180, NP_001311181, NP_001311182, NP_001311183, NP_001311185, NP_001311186, NP_001311187, NP_001311188, NP_001311189, NP_001311190, NP_001311191, NP_003412 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (15 total): zinc finger region 12, chain 1, domain 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P17032-F164.290.22

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 99 (showing top): BROWNE_HCMV_INFECTION_16HR_UP, BROWNE_HCMV_INFECTION_12HR_UP, DODD_NASOPHARYNGEAL_CARCINOMA_UP, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, chr10p11, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, ZWANG_DOWN_BY_2ND_EGF_PULSE, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ARID5B_TARGET_GENES, E2F5_TARGET_GENES, KAT2A_TARGET_GENES, KAT5_TARGET_GENES, SALL4_TARGET_GENES, ZBTB18_TARGET_GENES, ZNF331_TARGET_GENES

GO Biological Process (2): regulation of DNA-templated transcription (GO:0006355), regulation of transcription by RNA polymerase II (GO:0006357)

GO Molecular Function (6): RNA polymerase II cis-regulatory region sequence-specific DNA binding (GO:0000978), DNA-binding transcription factor activity, RNA polymerase II-specific (GO:0000981), DNA-binding transcription factor activity (GO:0003700), zinc ion binding (GO:0008270), DNA binding (GO:0003677), metal ion binding (GO:0046872)

GO Cellular Component (1): nucleus (GO:0005634)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
RNA Polymerase II Transcription1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of DNA-templated transcription2
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transcription by RNA polymerase II1
cis-regulatory region sequence-specific DNA binding1
chromatin1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transcription cis-regulatory region binding1
transcription regulator activity1
transition metal ion binding1
nucleic acid binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

592 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF37APLCB4Q15147429
ZNF37AC18orf32Q8TCD1336
ZNF37AMOGAT3Q86VF5322
ZNF37AMTRNR2L7P0CJ74308
ZNF37AZNF518AQ6AHZ1305
ZNF37AKNOP1Q1ED39290
ZNF37ATBC1D2BQ9UPU7266
ZNF37AGPATCH3Q96I76265
ZNF37ABANPQ8N9N5264
ZNF37AASAP3Q8TDY4261
ZNF37ASLC25A1P53007249
ZNF37AYPEL1O60688248
ZNF37ACELA2BP08218248
ZNF37APIGWQ7Z7B1247
ZNF37ANSRP1Q9H0G5245

IntAct

3 interactions, top by confidence:

ABTypeScore
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ZNF37AH1-2psi-mi:“MI:0915”(physical association)0.400

BioGRID (6): ZNF37A (Proximity Label-MS), ZNF37A (Negative Genetic), ZNF37A (Affinity Capture-MS), ZNF37A (Affinity Capture-MS), ZNF37A (Affinity Capture-RNA), ZNF37A (Proximity Label-MS)

ESM2 similar proteins: A2VDP4, A6NHJ4, O94892, P0CJ79, P17014, P17021, P17025, P17032, P17035, P18733, P51508, P51814, Q06730, Q06732, Q09FC8, Q0VGE8, Q14586, Q32M78, Q3MIS6, Q5JVG2, Q5R4K8, Q5R9S5, Q5RBQ3, Q5RCJ2, Q5RER9, Q5TYW1, Q5VIY5, Q6P560, Q6PDB4, Q6ZMW2, Q6ZN06, Q6ZNA1, Q76KX8, Q7L2R6, Q86Y25, Q8N184, Q8N823, Q8N883, Q8N8J6, Q8NEP9

Diamond homologs: A0A1W2PQL4, A0JNB1, A0JPL0, A6NK53, A6QLU5, A6QPT6, A7MBI1, A8MT65, A8MUV8, A8MWA4, B2RXC5, B4DU55, B4DX44, E9PYI1, O14628, O75346, P0CH99, P0CI00, P17014, P17030, P17032, P17098, P51786, P85977, Q02386, Q06730, Q06732, Q0VAW7, Q12901, Q13360, Q14586, Q14588, Q14590, Q16587, Q2M3X9, Q2VY69, Q32M78, Q3ZCX4, Q49AA0, Q4R6J4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance80
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1184 predictions. Top by Δscore:

VariantEffectΔscore
10:38095630:GTCT:Gdonor_gain1.0000
10:38095742:A:AGacceptor_gain1.0000
10:38095743:G:GGacceptor_gain1.0000
10:38095743:GA:Gacceptor_gain1.0000
10:38095800:ACAGA:Adonor_gain1.0000
10:38095801:CAGA:Cdonor_gain1.0000
10:38095803:GA:Gdonor_gain1.0000
10:38095803:GAGTA:Gdonor_loss1.0000
10:38095805:G:GGdonor_gain1.0000
10:38095805:GTAA:Gdonor_loss1.0000
10:38096565:A:AGacceptor_gain1.0000
10:38096566:T:Gacceptor_gain1.0000
10:38096569:CTCA:Cacceptor_loss1.0000
10:38096570:TCA:Tacceptor_loss1.0000
10:38096572:A:AGacceptor_gain1.0000
10:38096573:G:GAacceptor_gain1.0000
10:38096573:GC:Gacceptor_gain1.0000
10:38096573:GCT:Gacceptor_gain1.0000
10:38096573:GCTA:Gacceptor_gain1.0000
10:38096573:GCTAC:Gacceptor_gain1.0000
10:38096628:CCCAG:Cdonor_gain1.0000
10:38096629:CCAG:Cdonor_gain1.0000
10:38096630:CAG:Cdonor_gain1.0000
10:38096630:CAGG:Cdonor_loss1.0000
10:38096631:AG:Adonor_gain1.0000
10:38096632:GG:Gdonor_gain1.0000
10:38096633:G:GGdonor_gain1.0000
10:38096633:GTAA:Gdonor_loss1.0000
10:38114878:GTAG:Gdonor_gain1.0000
10:38115193:AG:Aacceptor_gain1.0000

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS1000040282 (10:38098503 A>C), RS1000187954 (10:38121512 A>G), RS1000235619 (10:38125047 C>T), RS1000406570 (10:38118683 T>C), RS1000508440 (10:38138946 A>T), RS1000700410 (10:38131564 T>C), RS1000889491 (10:38113031 C>T), RS1000921290 (10:38094388 T>C), RS1000922072 (10:38113317 A>G), RS1001049868 (10:38145370 A>G), RS1001062916 (10:38145673 T>C), RS1001221117 (10:38117673 C>A), RS1001369120 (10:38104270 C>A,T), RS1001533824 (10:38131164 T>C), RS1001551288 (10:38106210 G>T)

Disease associations

OMIM: gene MIM:616085 | disease phenotypes:

GenCC curated gene-disease

DiseaseClassificationInheritance
Tourette syndromeNo Known Disease RelationshipUnknown

Mondo (1): Tourette syndrome (MONDO:0007661)

Orphanet (0):

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST010919_4QT interval2.000000e-10

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004682QT interval

MeSH disease descriptors (1)

DescriptorNameTree numbers
D005879Tourette SyndromeC10.228.140.079.898; C10.228.662.825.800; C10.574.500.850; C16.320.400.820; F03.625.992.850

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

36 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
GSK-J4decreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
bisphenol Aincreases expression1
dimethylselenideincreases oxidation, decreases expression, increases expression1
arseniteaffects binding, decreases reaction1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
potassium chromate(VI)affects cotreatment, increases expression1
ferrous chloridedecreases expression1
cupric oxideincreases expression1
epigallocatechin gallateincreases expression, affects cotreatment1
avobenzonedecreases expression1
perfluorooctane sulfonic aciddecreases expression1
pentabromodiphenyl etherdecreases expression1
K 7174increases expression1
abrinedecreases expression1
jinfukangdecreases expression1
Resveratrolaffects cotreatment, increases expression1
Sunitinibincreases expression1
Arsenic Trioxideincreases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Aspirinincreases expression1
Benzo(a)pyreneaffects methylation1
Caffeineincreases expression1
Cisplatindecreases expression1
Ethyl Methanesulfonateincreases expression1
Formaldehydeincreases expression1
Glucoseincreases expression1
Methyl Methanesulfonateincreases expression1
Plant Extractsaffects cotreatment, increases expression1

Clinical trials (associated diseases)

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

TrialPhaseStatusTitle
NCT00152750PHASE4UNKNOWNStudy of Clonidine on Sleep Architecture in Children With Tourette’s Syndrome (TS) and Comorbid ADHD
NCT00226824PHASE4TERMINATEDSafety Study of Galantamine in Tic Disorders
NCT00241176PHASE4COMPLETEDOpen Label Trial of Aripiprazole in Children and Adolescents With Tourette’s Disorder
NCT00370838PHASE4COMPLETEDComparison of Keppra and Clonidine in the Treatment of Tics
NCT01018056PHASE4COMPLETEDDeveloping New Treatments for Tourette Syndrome: Therapeutic Trials With Modulators of Glutamatergic Neurotransmission
NCT01547000PHASE4COMPLETEDGuanfacine in Children With Tic Disorders
NCT03239210PHASE4COMPLETEDEffects of Ondansetron in Obsessive-compulsive and Tic Disorders
NCT00004376PHASE3COMPLETEDPhase III Randomized, Double-Blind, Placebo-Controlled Study of Guanfacine for Tourette Syndrome and Attention Deficit Hyperactivity Disorder
NCT00206323PHASE3COMPLETEDA Randomized, Placebo-controlled, Tourette Syndrome Study.
NCT00206336PHASE3COMPLETEDAn Open-label Study to Determine the Efficacy and Safety of Topiramate in the Treatment of Tourette Syndrome.
NCT00478842PHASE3COMPLETEDPallidal Stimulation and Gilles de la Tourette Syndrome
NCT00681863PHASE3TERMINATEDOpen-label Extension Study of Pramipexole in the Treatment of Children and Adolescents With Tourette Syndrome
NCT01501695PHASE3COMPLETEDPhase III Study of 5LGr to Treat Tic Disorder
NCT03087201PHASE3COMPLETEDCANNAbinoids in the Treatment of TICS (CANNA-TICS)
NCT03487783PHASE3COMPLETEDAripiprazole Oral Solution in the Treatment of Children and Adolescents With Tourette’s Syndrome
NCT03567291PHASE3TERMINATEDEvaluation of Safety and Tolerability of Long-term TEV-50717 (Deutetrabenazine) for Treatment of Tourette Syndrome in Children and Adolescents
NCT03571256PHASE3COMPLETEDA Study to Test if TEV-50717 is Effective in Relieving Tics Associated With Tourette Syndrome (TS)
NCT06021522PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate Long-term Safety of Ecopipam Tablets in Children, Adolescents and Adults With Tourette’s Disorder
NCT00004393PHASE2COMPLETEDPhase II Double Blind Placebo Controlled Trial of Risperidone in Tourette Syndrome
NCT00004652PHASE2COMPLETEDPhase II Pilot Controlled Study of Short Vs Longer Term Pimozide (Orap) Therapy in Tourette Syndrome
NCT00231985PHASE2COMPLETEDEffectiveness of Behavior Therapy and Psychosocial Therapy for the Treatment of Tourette Syndrome and Chronic Tic Disorder
NCT00311909PHASE2COMPLETEDThalamic Deep Brain Stimulation for Tourette Syndrome
NCT00529308PHASE2COMPLETEDTranscranial Magnetic Stimulation (TMS) for Individuals With Tourette’s Syndrome
NCT00558467PHASE2COMPLETEDPramipexole Pilot Phase II Study in Children and Adolescents With Tourette Disorder According to DSM-IV Criteria
NCT01043549PHASE2TERMINATEDRepetitive Transcranial Magnetic Stimulation of the Posterior Parietal Cortex in Patients Suffering From Gilles de la Tourette Syndrome
NCT01133353PHASE2WITHDRAWNA Study of the Effectiveness and Safety of Tetrabenazine MR in Pediatric Subjects With Tourette’s Syndrome
NCT01475383PHASE2WITHDRAWNStudy Evaluating The Safety And Efficacy Of PF-03654746 In Adult Subjects With Tourette’s Syndrome
NCT01647269PHASE2COMPLETEDA Trial of Bilateral Deep Brain Stimulation to the Globus Pallidus Internum in Tourette Syndrome
NCT01904773PHASE2COMPLETEDSafety, Tolerability, Pharmacokinetic, and Efficacy Study of AZD5213 in Adolescents With Tourette’s Disorder
NCT02102698PHASE2COMPLETEDEcopipam Treatment of Tourette’s Syndrome in Subjects 7-17 Years
NCT02217007PHASE2WITHDRAWNA Trial Evaluating the Efficacy, Safety, and Pharmacokinetics of SNC-102 in Subjects With Tourette Syndrome
NCT02247206PHASE2COMPLETEDVoIP Delivered Behavior Therapy for Tourette Syndrome
NCT02581865PHASE2COMPLETEDSafety and Efficacy Study of NBI-98854 in Adults With Tourette Syndrome
NCT02619084PHASE2COMPLETEDSubthalamic Stimulation in Tourette’s Syndrome
NCT02679079PHASE2COMPLETEDSafety and Efficacy Study of NBI-98854 in Children and Adolescents With Tourette Syndrome
NCT02879578PHASE2COMPLETEDSafety and Tolerability Study of NBI-98854 for the Treatment of Subjects With Tourette Syndrome
NCT03066193PHASE2COMPLETEDEfficacy of a Therapeutic Combination of Dronabinol and PEA for Tourette Syndrome
NCT03247244PHASE2TERMINATEDSafety and Efficacy of Cannabis in Tourette Syndrome
NCT03325010PHASE2COMPLETEDSafety, Tolerability, and Efficacy of NBI-98854 for the Treatment of Pediatric Subjects With Tourette Syndrome
NCT03444038PHASE2COMPLETEDOpen-Label Safety and Tolerability Study of NBI-98854 for the Treatment of Pediatric Subjects With Tourette Syndrome
  • Associated diseases: Tourette syndrome
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): Tourette syndrome