STK32C

gene
On this page

Also known as PKEMGC23665YANK3

Summary

STK32C (serine/threonine kinase 32C, HGNC:21332) is a protein-coding gene on chromosome 10q26.3, encoding Serine/threonine-protein kinase 32C (Q86UX6).

The protein encoded by this gene is a member of the serine/threonine protein kinase family. It is thought that this family member is functional in brain due to its high expression levels there. DNA methylation differences have been found in this gene in monozygotic twins that are discordant for adolescent depression. Alternative splicing results in multiple transcript variants.

Source: NCBI Gene 282974 — RefSeq curated summary.

At a glance

  • GWAS associations: 5
  • Clinical variants (ClinVar): 79 total — 1 pathogenic
  • Druggable target: yes — 1 molecules with ChEMBL bioactivity
  • MANE Select transcript: NM_173575

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:21332
Approved symbolSTK32C
Nameserine/threonine kinase 32C
Location10q26.3
Locus typegene with protein product
StatusApproved
AliasesPKE, MGC23665, YANK3
Ensembl geneENSG00000165752
Ensembl biotypeprotein_coding
OMIM621308
Entrez282974

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 8 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000298630, ENST00000368619, ENST00000368620, ENST00000368622, ENST00000456004, ENST00000462160, ENST00000858942, ENST00000916800, ENST00000956240

RefSeq mRNA: 6 — MANE Select: NM_173575 NM_001318878, NM_001318879, NM_001318880, NM_001318881, NM_001318883, NM_173575

CCDS: CCDS7666, CCDS81525, CCDS81526, CCDS81527

Canonical transcript exons

ENST00000298630 — 12 exons

ExonStartEnd
ENSE00001268023132307572132307950
ENSE00001610205132225527132225616
ENSE00001660695132225233132225336
ENSE00003350665132222641132222772
ENSE00003353212132224407132224523
ENSE00003373424132226795132226968
ENSE00003412781132222861132222986
ENSE00003423588132225747132225784
ENSE00003546748132207492132208151
ENSE00003627843132209034132209101
ENSE00003688899132227977132228128
ENSE00003692390132245900132245955

Expression profiles

Bgee: expression breadth ubiquitous, 198 present calls, max score 94.68.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 12.2279 / max 297.4962, expressed in 1798 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
1120644.70371469
1120664.38531657
1120671.99211198
1120630.8615408
1120680.2853125

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right testisUBERON:000453494.68gold quality
left testisUBERON:000453394.62gold quality
anterior cingulate cortexUBERON:000983593.56gold quality
right frontal lobeUBERON:000281093.30gold quality
Brodmann (1909) area 9UBERON:001354093.09gold quality
dorsolateral prefrontal cortexUBERON:000983492.26gold quality
prefrontal cortexUBERON:000045192.05gold quality
testisUBERON:000047391.67gold quality
caudate nucleusUBERON:000187390.92gold quality
amygdalaUBERON:000187690.91gold quality
putamenUBERON:000187490.75gold quality
nucleus accumbensUBERON:000188290.71gold quality
neocortexUBERON:000195090.46gold quality
frontal cortexUBERON:000187090.41gold quality
pancreatic ductal cellCL:000207990.34silver quality
cerebral cortexUBERON:000095689.26gold quality
hypothalamusUBERON:000189888.12gold quality
forebrainUBERON:000189088.11gold quality
monocyteCL:000057688.09gold quality
leukocyteCL:000073887.65gold quality
C1 segment of cervical spinal cordUBERON:000646987.15gold quality
middle temporal gyrusUBERON:000277187.00gold quality
brainUBERON:000095586.84gold quality
temporal lobeUBERON:000187186.82gold quality
Ammon’s hornUBERON:000195486.72gold quality
granulocyteCL:000009485.26gold quality
spermCL:000001985.21silver quality
right hemisphere of cerebellumUBERON:001489085.07gold quality
spinal cordUBERON:000224084.99gold quality
left adrenal gland cortexUBERON:003582584.92gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.29

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

13 targeting STK32C, 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-6508-5P99.9270.672465
HSA-MIR-806799.8669.592260
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-6766-5P99.6867.702325
HSA-MIR-5571-5P99.4966.991764
HSA-MIR-608199.4866.071446
HSA-MIR-7854-3P99.0866.261117
HSA-MIR-3135B98.6165.331470
HSA-MIR-429098.5165.17907
HSA-MIR-425797.8668.051190
HSA-MIR-466097.7967.441328
HSA-MIR-517-5P97.1368.43781
HSA-MIR-6784-5P84.5660.91126

Literature-anchored findings (GeneRIF, showing 1)

  • Silencing of STK32C inhibited the activity of the HMGB1 pathway and regulated the expression of key genes in this pathway. (PMID:30359551)

Cross-species orthologs

8 orthologs

OrganismSymbolGene ID
mus_musculusStk32cENSMUSG00000015981
rattus_norvegicusStk32cENSRNOG00000006962
drosophila_melanogasterCG32944FBGN0052944
drosophila_melanogasterdopFBGN0267390
caenorhabditis_elegansWBGENE00002192
caenorhabditis_eleganswts-1WBGENE00007047
caenorhabditis_elegansWBGENE00010838
caenorhabditis_elegansWBGENE00011992

Paralogs (13): MAST4 (ENSG00000069020), MAST2 (ENSG00000086015), MAST3 (ENSG00000099308), SGK2 (ENSG00000101049), SGK3 (ENSG00000104205), DMPK (ENSG00000104936), MAST1 (ENSG00000105613), SGK1 (ENSG00000118515), MASTL (ENSG00000120539), LATS1 (ENSG00000131023), LATS2 (ENSG00000150457), STK32B (ENSG00000152953), STK32A (ENSG00000169302)

Protein

Protein identifiers

Serine/threonine-protein kinase 32CQ86UX6 (reviewed: Q86UX6)

Alternative names: PKE, Yet another novel kinase 3

All UniProt accessions (5): A0A0A0MRK9, A0A140VJW0, Q86UX6, H0Y349, H0Y431

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the protein kinase superfamily. Ser/Thr protein kinase family.

Isoforms (2)

UniProt IDNamesCanonical?
Q86UX6-11yes
Q86UX6-22

RefSeq proteins (6): NP_001305807, NP_001305808, NP_001305809, NP_001305810, NP_001305812, NP_775846* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000719Prot_kinase_domDomain
IPR008271Ser/Thr_kinase_ASActive_site
IPR011009Kinase-like_dom_sfHomologous_superfamily
IPR017441Protein_kinase_ATP_BSBinding_site

Pfam: PF00069

Catalyzed reactions (Rhea), 2 shown:

  • L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H(+) (RHEA:17989)
  • L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H(+) (RHEA:46608)

UniProt features (19 total): sequence variant 5, modified residue 3, region of interest 3, compositionally biased region 2, binding site 2, chain 1, domain 1, splice variant 1, active site 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q86UX6-F179.950.59

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Catalytic / active sites (1): 216 (proton acceptor)

Ligand- & substrate-binding residues (2): 99–107; 122

Post-translational modifications (3): 10, 15, 18

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 80 (showing top): TGACATY_UNKNOWN, GOMF_PROTEIN_KINASE_ACTIVITY, GOMF_KINASE_ACTIVITY, YKACATTT_UNKNOWN, GOMF_PROTEIN_SERINE_THREONINE_KINASE_ACTIVITY, DODD_NASOPHARYNGEAL_CARCINOMA_DN, GOMF_ADENYL_NUCLEOTIDE_BINDING, HMGIY_Q6, GOMF_TRANSFERASE_ACTIVITY_TRANSFERRING_PHOSPHORUS_CONTAINING_GROUPS, MEISSNER_NPC_HCP_WITH_H3K4ME3_AND_H3K27ME3, MIKKELSEN_MCV6_HCP_WITH_H3K27ME3, MIKKELSEN_NPC_HCP_WITH_H3K4ME3_AND_H3K27ME3, DUAN_PRDM5_TARGETS, DACH1_TARGET_GENES, FOXJ2_TARGET_GENES

GO Biological Process (2): intracellular signal transduction (GO:0035556), protein phosphorylation (GO:0006468)

GO Molecular Function (9): protein serine/threonine kinase activity (GO:0004674), ATP binding (GO:0005524), metal ion binding (GO:0046872), protein serine kinase activity (GO:0106310), nucleotide binding (GO:0000166), protein kinase activity (GO:0004672), protein binding (GO:0005515), kinase activity (GO:0016301), transferase activity (GO:0016740)

GO Cellular Component (0):

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein kinase activity2
intracellular anatomical structure1
signal transduction1
phosphorylation1
protein modification process1
adenyl ribonucleotide binding1
purine ribonucleoside triphosphate binding1
cation binding1
nucleoside phosphate binding1
heterocyclic compound binding1
kinase activity1
phosphotransferase activity, alcohol group as acceptor1
catalytic activity, acting on a protein1
binding1
transferase activity, transferring phosphorus-containing groups1
catalytic activity1

Protein interactions and networks

STRING

832 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
STK32CMCF2LO15068503
STK32CLRRC8BQ6P9F7486
STK32CCCDC144AA2RUR9384
STK32CLMTK2Q8IWU2339
STK32CINPP5AQ14642335
STK32CCEP170BQ9Y4F5332
STK32CZNF329Q86UD4326
STK32CYIPF1Q9Y548315
STK32CCCDC33Q8N5R6309
STK32CPPP1R21Q6ZMI0300
STK32CMFSD11O43934295
STK32CTMUB2Q71RG4295
STK32CFAM110AQ9BQ89295
STK32CNME8Q8N427294
STK32CNUP210LQ5VU65290

IntAct

15 interactions, top by confidence:

ABTypeScore
HGSSTK32Cpsi-mi:“MI:0915”(physical association)0.560
STK32CHSP90AB1psi-mi:“MI:0915”(physical association)0.560
STK32CFDFT1psi-mi:“MI:0914”(association)0.530
YWHAESTK32Cpsi-mi:“MI:0915”(physical association)0.400
SFNSTK32Cpsi-mi:“MI:0915”(physical association)0.400
STK32CSHANK3psi-mi:“MI:0915”(physical association)0.370
STK32CILVBLpsi-mi:“MI:0914”(association)0.350
PHF10NVLpsi-mi:“MI:0914”(association)0.350
STK32CHAUS5psi-mi:“MI:0914”(association)0.350
RPRMSTK32Cpsi-mi:“MI:0915”(physical association)0.000
HGSSTK32Cpsi-mi:“MI:0915”(physical association)0.000
STK32CGRB2psi-mi:“MI:0915”(physical association)0.000

BioGRID (95): HSP90AA5P (Affinity Capture-MS), HSP90AA4P (Affinity Capture-MS), FDFT1 (Affinity Capture-MS), CDC37 (Affinity Capture-MS), MCM5 (Affinity Capture-MS), HSP90AA5P (Affinity Capture-MS), HSP90AA4P (Affinity Capture-MS), STK32C (Affinity Capture-RNA), HGS (Two-hybrid), STK32C (Two-hybrid), HSP90AA4P (Affinity Capture-MS), FDFT1 (Affinity Capture-MS), HSP90AA5P (Affinity Capture-MS), HAUS3 (Affinity Capture-MS), IQGAP3 (Affinity Capture-MS)

ESM2 similar proteins: A5PKJ4, B2DD29, B8Y466, O14976, O43781, O54781, O60307, O70551, O88831, P0C865, P33279, P78362, P97756, Q13164, Q20443, Q3U214, Q3V016, Q4R6S5, Q4R8E0, Q4V793, Q4V8A3, Q5RD27, Q5RJI5, Q641K5, Q84M93, Q86UX6, Q8C078, Q8CIP4, Q8N5S9, Q8NE63, Q8QZV4, Q8TD08, Q8TDC3, Q8VBY2, Q8WP28, Q922Y0, Q96L34, Q96RR4, Q96SB4, Q99KY4

Diamond homologs: A1Z9X0, A2VDZ4, A7MB74, A8XJQ6, A8XNJ6, B2GUY1, B4IMC3, B4NSS9, F1M7Y5, F4HPN2, F4JY37, J9W0G9, M3TYT0, O00141, O15530, O55173, O70291, O74426, O75116, O77819, P05130, P09216, P10666, P10830, P11792, P12370, P13678, P16054, P18654, P23298, P25341, P26818, P28178, P28327, P32866, P34099, P34102, P34103, P34885, P36582

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic1
Likely pathogenic0
Uncertain significance59
Likely benign4
Benign5

Top pathogenic / likely-pathogenic (1)

Variant IDHGVSClassification
1077185Single allelePathogenic

SpliceAI

3919 predictions. Top by Δscore:

VariantEffectΔscore
10:132209029:CTCA:Cdonor_gain1.0000
10:132209031:CA:Cdonor_loss1.0000
10:132209032:A:ACdonor_gain1.0000
10:132209033:C:CTdonor_gain1.0000
10:132209033:CT:Cdonor_gain1.0000
10:132209033:CTTTT:Cdonor_gain1.0000
10:132209097:TTCTC:Tacceptor_gain1.0000
10:132209099:CTC:Cacceptor_gain1.0000
10:132209100:TC:Tacceptor_gain1.0000
10:132209101:CC:Cacceptor_gain1.0000
10:132209101:CCTGT:Cacceptor_loss1.0000
10:132209102:C:CCacceptor_gain1.0000
10:132209103:T:Gacceptor_loss1.0000
10:132222640:CGGA:Cdonor_gain1.0000
10:132222773:C:CCacceptor_gain1.0000
10:132222859:A:ACdonor_gain1.0000
10:132222860:C:CCdonor_gain1.0000
10:132222860:CG:Cdonor_gain1.0000
10:132222983:GGAG:Gacceptor_gain1.0000
10:132222986:GC:Gacceptor_loss1.0000
10:132222987:C:CCacceptor_gain1.0000
10:132222987:CTG:Cacceptor_loss1.0000
10:132222988:T:Aacceptor_loss1.0000
10:132224401:GCTCA:Gdonor_loss1.0000
10:132224402:CTCA:Cdonor_loss1.0000
10:132224403:TCA:Tdonor_loss1.0000
10:132224406:C:CGdonor_loss1.0000
10:132224522:CT:Cacceptor_gain1.0000
10:132225617:C:CCacceptor_gain1.0000
10:132226792:CACC:Cdonor_loss1.0000

AlphaMissense

3213 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:132222726:A:CI389S1.000
10:132222726:A:GI389T1.000
10:132222726:A:TI389N1.000
10:132222735:T:AE386V1.000
10:132222738:A:GL385P1.000
10:132222738:A:TL385Q1.000
10:132225265:C:AG282W1.000
10:132225274:A:GW279R1.000
10:132225274:A:TW279R1.000
10:132225541:G:AT253I1.000
10:132225544:C:TG252D1.000
10:132225586:G:TA238D1.000
10:132225591:G:CN236K1.000
10:132225591:G:TN236K1.000
10:132225597:G:CD234E1.000
10:132225597:G:TD234E1.000
10:132225598:T:AD234V1.000
10:132225598:T:CD234G1.000
10:132225598:T:GD234A1.000
10:132225599:C:GD234H1.000
10:132225616:C:TG228E1.000
10:132225761:A:GL223P1.000
10:132225766:G:CN221K1.000
10:132225766:G:TN221K1.000
10:132225775:C:AK218N1.000
10:132225775:C:GK218N1.000
10:132225777:T:CK218E1.000
10:132225781:A:CD216E1.000
10:132225781:A:TD216E1.000
10:132225782:T:AD216V1.000

dbSNP variants (sampled 300 via entrez): RS1000012358 (10:132331176 G>A), RS1000015664 (10:132236556 C>A), RS1000031320 (10:132216243 T>C), RS1000045057 (10:132330810 TA>T,TAA), RS1000065733 (10:132321055 A>G), RS1000088634 (10:132211226 G>A), RS1000128260 (10:132270116 C>G,T), RS1000170700 (10:132244309 C>T), RS1000200533 (10:132232823 G>A,C), RS1000218795 (10:132231179 G>C,T), RS1000249009 (10:132236860 G>A,T), RS1000249321 (10:132297264 T>A,C), RS1000249892 (10:132207882 C>T), RS1000290184 (10:132211738 T>C), RS1000297768 (10:132236731 C>A,T)

Disease associations

OMIM: gene MIM:621308 | disease phenotypes: MIM:609625

GenCC curated gene-disease

Mondo (1): distal 10q deletion syndrome (MONDO:0012315)

Orphanet (1): Distal deletion 10q syndrome (Orphanet:96148)

HPO phenotypes

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

GWAS associations

5 associations (top):

StudyTraitp-value
GCST006460_9Bronchopulmonary dysplasia in preterm infants3.000000e-06
GCST007325_259General risk tolerance (MTAG)3.000000e-09
GCST007325_9General risk tolerance (MTAG)7.000000e-09
GCST008181_10Spontaneous preterm birth without premature rupture of membranes7.000000e-06
GCST009082_1Pneumococcal meningitis x streptococcus pneumoniae genotype cluster interaction1.000000e-08

EFO canonical traits (3, from GWAS)

EFO IDTrait name
EFO:0008579risk-taking behaviour
EFO:0006917spontaneous preterm birth
EFO:0010271bacterial pathogen genotype measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
C567182Chromosome 10q26 Deletion Syndrome (supp.)

Drugs & pharmacology

Drug and pharmacology data

Is drug target: yes

ChEMBL targets (1): CHEMBL5405 (SINGLE PROTEIN)

Molecules with ChEMBL bioactivity

1 molecules (phase ≥1), by development phase (incl. off-target/promiscuous compounds).

MoleculeNamePhasePatents
CHEMBL603469LESTAURTINIB3

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

GtoPdb / IUPHAR curated pharmacology

(IUPHAR/BPS Guide to Pharmacology — expert-curated)

Target class: enzyme — YANK family

ChEMBL bioactivities

12 potent at pChembl≥5 of 12 total, top 11 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).

pChemblTypeValueUnitMolecule
7.26Kd55nMTAE-684
6.86IC50139nMSTAUROSPORINE
6.79IC50162nMSTAUROSPORINE
6.51Kd310nMSTAUROSPORINE
6.49Kd326nMCHEMBL4576489
6.49IC50325nMSTAUROSPORINE
6.35Kd448nMCHEMBL4465866
6.00IC501000nMTP-030-1
6.00IC501000nMTP-030-2
6.00IC501000nMTP-030n
5.10Kd8000nMLESTAURTINIB

PubChem BioAssay actives

9 with measured affinity, of 262 total; 5 most potent distinct compounds. Largely complementary to BindingDB; screening values are coarse (µM, 4 dp), so sub-nM hits tie at the floor.

CompoundAssayTypeValueUnit
5-chloro-2-N-[2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]-4-N-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine624734: Binding constant for YANK3 kinase domainkd0.0550uM
(2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-29-oxa-1,7,17-triazaoctacyclo[12.12.2.12,6.07,28.08,13.015,19.020,27.021,26]nonacosa-8,10,12,14,19,21,23,25,27-nonaen-16-one1715156: Inhibition of human STK32C using MBP as substrate by [gamma-33P]-ATP assayic500.1390uM
3-(2,2-difluoro-10,12-dimethyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-4-yl)-N-[2-[2-[2-[2-[[(2S,3R,4R,6R)-3-methoxy-2-methyl-16-oxo-29-oxa-1,7,17-triazaoctacyclo[12.12.2.12,6.07,28.08,13.015,19.020,27.021,26]nonacosa-8,10,12,14,19,21,23,25,27-nonaen-4-yl]-methylamino]ethoxy]ethoxy]ethoxy]ethyl]propanamide1526275: Binding affinity to recombinant full-length N-terminal His-FLAG-GST-tagged STK32C (unknown origin) (66 to 486 residues) expressed in baculovirus infected Sf9 insect cells incubated for 1 hr by TR-FRET assaykd0.3260uM
3-(2,2-difluoro-10,12-dimethyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-4-yl)-N-[2-[2-[2-[2-[[(2S,3R,4R,6R)-3-methoxy-2-methyl-16-oxo-29-oxa-1,7,17-triazaoctacyclo[12.12.2.12,6.07,28.08,13.015,19.020,27.021,26]nonacosa-8,10,12,14,19,21,23,25,27-nonaen-4-yl]amino]ethoxy]ethoxy]ethoxy]ethyl]propanamide1526275: Binding affinity to recombinant full-length N-terminal His-FLAG-GST-tagged STK32C (unknown origin) (66 to 486 residues) expressed in baculovirus infected Sf9 insect cells incubated for 1 hr by TR-FRET assaykd0.4480uM
(15S,16S,18R)-16-hydroxy-16-(hydroxymethyl)-15-methyl-28-oxa-4,14,19-triazaoctacyclo[12.11.2.115,18.02,6.07,27.08,13.019,26.020,25]octacosa-1,6,8,10,12,20,22,24,26-nonaen-3-one624734: Binding constant for YANK3 kinase domainkd8.0000uM

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, decreases expression, increases methylation3
trichostatin Aaffects cotreatment, decreases expression, affects expression2
Valproic Acidaffects expression, increases methylation2
bisphenol Aaffects cotreatment, increases methylation, decreases methylation1
beta-lapachonedecreases expression1
sodium arsenitedecreases expression1
butyraldehydeincreases expression1
benzo(e)pyreneincreases methylation, decreases methylation1
aflatoxin B2decreases methylation, increases methylation1
avobenzoneincreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
2-palmitoylglycerolincreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphindecreases expression, affects cotreatment1
bisphenol Sdecreases methylation1
jinfukangincreases expression1
Fulvestrantaffects cotreatment, increases methylation1
Caffeinedecreases phosphorylation1
Diethylhexyl Phthalatedecreases expression1
Estradiolincreases expression1
Methapyrilenedecreases methylation, increases methylation1
Smokedecreases expression1
Urethaneincreases expression1
Aflatoxin B1increases methylation1
Asbestos, Serpentineincreases methylation1
Asbestos, Crocidoliteincreases methylation1
Cadmium Chlorideincreases expression1
Okadaic Acidincreases expression1
Acrylamideincreases expression1

ChEMBL screening assays

148 unique, capped per target: 148 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL1043385BindingBinding affinity to human YANK3 at 500 nM by cell-based competition binding assay relative to control in presence of DTTStaurosporine tethered peptide ligands that target cAMP-dependent protein kinase (PKA): optimization and selectivity profiling. — Bioorg Med Chem

Cellosaurus cell lines

2 cell lines: 2 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_TQ88HAP1 STK32C (-) 1Cancer cell lineMale
CVCL_TQ89HAP1 STK32C (-) 2Cancer cell lineMale

Clinical trials (associated diseases)

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