CA11

gene
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Also known as CARP2CARPX1

Summary

CA11 (carbonic anhydrase 11 (inactive), HGNC:1370) is a protein-coding gene on chromosome 19q13.33, encoding Carbonic anhydrase-related protein 11 (O75493). Does not have a catalytic activity.

Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. They participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. They show extensive diversity in tissue distribution and in their subcellular localization. CA XI is likely a secreted protein, however, radical changes at active site residues completely conserved in CA isozymes with catalytic activity, make it unlikely that it has carbonic anhydrase activity. It shares properties in common with two other acatalytic CA isoforms, CA VIII and CA X. CA XI is most abundantly expressed in brain, and may play a general role in the central nervous system.

Source: NCBI Gene 770 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 44 total
  • Druggable target: yes — 1 molecules with ChEMBL bioactivity
  • MANE Select transcript: NM_001217

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:1370
Approved symbolCA11
Namecarbonic anhydrase 11 (inactive)
Location19q13.33
Locus typegene with protein product
StatusApproved
AliasesCARP2, CARPX1
Ensembl geneENSG00000063180
Ensembl biotypeprotein_coding
OMIM604644
Entrez770

Gene structure

Transcript identifiers

Ensembl transcripts: 9 — 7 protein_coding, 2 retained_intron

ENST00000084798, ENST00000594088, ENST00000596080, ENST00000599267, ENST00000901033, ENST00000901034, ENST00000901035, ENST00000901036, ENST00000901037

RefSeq mRNA: 1 — MANE Select: NM_001217 NM_001217

CCDS: CCDS12729

Canonical transcript exons

ENST00000084798 — 9 exons

ExonStartEnd
ENSE000007178554864540348645477
ENSE000007178564864442748644569
ENSE000007178584863978848639883
ENSE000007178604863954948639621
ENSE000007178634863930548639459
ENSE000008629324864009548640280
ENSE000008629334863888848639053
ENSE000012404064864556648646187
ENSE000031386884863794648638144

Expression profiles

Bgee: expression breadth ubiquitous, 254 present calls, max score 99.74.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 11.0105 / max 1248.7644, expressed in 1225 samples.

FANTOM5 promoters (11 alternative TSS)

Promoter IDTPM avgSamples expressed
1819053.6204438
1819082.0004418
1818961.5171462
1819101.3317500
1819091.3024450
1819020.5326169
1819010.2710120
1818950.195295
1819040.087144
1819030.079537

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right hemisphere of cerebellumUBERON:001489099.74gold quality
cerebellar hemisphereUBERON:000224599.70gold quality
cerebellar cortexUBERON:000212999.69gold quality
right frontal lobeUBERON:000281099.61gold quality
cerebellumUBERON:000203799.47gold quality
amygdalaUBERON:000187699.28gold quality
nucleus accumbensUBERON:000188299.28gold quality
caudate nucleusUBERON:000187399.27gold quality
dorsolateral prefrontal cortexUBERON:000983499.20gold quality
Brodmann (1909) area 9UBERON:001354099.18gold quality
prefrontal cortexUBERON:000045199.17gold quality
cingulate cortexUBERON:000302799.16gold quality
anterior cingulate cortexUBERON:000983599.14gold quality
putamenUBERON:000187499.12gold quality
frontal cortexUBERON:000187098.64gold quality
Brodmann (1909) area 10UBERON:001354198.34gold quality
temporal lobeUBERON:000187198.10gold quality
cerebellar vermisUBERON:000472098.02gold quality
neocortexUBERON:000195097.96gold quality
frontal poleUBERON:000279597.90gold quality
telencephalonUBERON:000189397.81gold quality
cerebral cortexUBERON:000095697.56gold quality
forebrainUBERON:000189097.37gold quality
Ammon’s hornUBERON:000195497.34gold quality
C1 segment of cervical spinal cordUBERON:000646997.30gold quality
brainUBERON:000095597.22gold quality
parietal lobeUBERON:000187297.19gold quality
central nervous systemUBERON:000101797.17gold quality
lateral globus pallidusUBERON:000247697.13gold quality
paraflocculusUBERON:000535197.13gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.93

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): NR1I2

miRNA regulators (miRDB)

9 targeting CA11, 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-318599.9968.121959
HSA-MIR-6888-3P99.9765.951170
HSA-MIR-6887-3P99.6667.831778
HSA-MIR-208A-5P99.4270.831913
HSA-MIR-208B-5P99.4270.831952
HSA-MIR-425199.4069.193363
HSA-MIR-26B-3P98.7167.491102
HSA-MIR-63398.3569.451167
HSA-MIR-6826-3P98.1966.321153

Literature-anchored findings (GeneRIF, showing 2)

  • The CARP VIII and XI proteins were associated to non-hypoxic conditions and CARP XI also to the expression of cytoplasmic CA II staining suggesting that the CARPs play a role in tumorigenesis of diffusively infiltrating gliomas (PMID:29792187)
  • results suggest that CA11 and CA10 negatively regulate neuronal activity-dependent glioma growth and inhibit glioma aggression. Thus, CA11/CA10 may represent a potential therapeutic target for the treatment of gliomas. (PMID:30636076)

Cross-species orthologs

18 orthologs

OrganismSymbolGene ID
danio_reriocahzENSDARG00000011166
danio_rerioca2ENSDARG00000014488
mus_musculusCar11ENSMUSG00000003273
rattus_norvegicusCar11ENSRNOG00000021017
drosophila_melanogasterCAH13FBGN0033542
drosophila_melanogasterCAH14FBGN0034554
drosophila_melanogasterCAH15FBGN0034560
drosophila_melanogasterCAH7FBGN0037788
drosophila_melanogasterCAH8FBGN0038956
drosophila_melanogasterCAH4FBGN0039235
drosophila_melanogasterCAH9FBGN0039486
drosophila_melanogasterCAH6FBGN0039838
drosophila_melanogasterCAH16FBGN0040628
drosophila_melanogasterCAH5FBGN0040629
drosophila_melanogasterCARPBFBGN0052698
caenorhabditis_elegansWBGENE00000279
caenorhabditis_elegansWBGENE00000283
caenorhabditis_eleganscah-6WBGENE00000284

Paralogs (14): CA12 (ENSG00000074410), CA2 (ENSG00000104267), CA9 (ENSG00000107159), CA14 (ENSG00000118298), CA6 (ENSG00000131686), CA1 (ENSG00000133742), CA10 (ENSG00000154975), CA3 (ENSG00000164879), CA4 (ENSG00000167434), CA7 (ENSG00000168748), CA5B (ENSG00000169239), CA5A (ENSG00000174990), CA8 (ENSG00000178538), CA13 (ENSG00000185015)

Protein

Protein identifiers

Carbonic anhydrase-related protein 11O75493 (reviewed: O75493)

Alternative names: CA-RP XI, Carbonic anhydrase-related protein 2

All UniProt accessions (2): O75493, M0QXK8

UniProt curated annotations — full annotation on UniProt →

Function. Does not have a catalytic activity.

Subcellular location. Secreted.

Tissue specificity. Expressed abundantly in the brain with moderate expression also present in spinal cord and thyroid.

Similarity. Belongs to the alpha-carbonic anhydrase family.

RefSeq proteins (1): NP_001208* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001148CA_domDomain
IPR023561Carbonic_anhydrase_a-classFamily
IPR036398CA_dom_sfHomologous_superfamily
IPR041878Alpha_CARP_X/XIFamily

Pfam: PF00194

UniProt features (11 total): sequence conflict 3, glycosylation site 3, signal peptide 1, chain 1, domain 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-O75493-F188.390.76

Functional residue map

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

Glycosylation sites (3): 118, 170, 260

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 119 (showing top): RRAGTTGT_UNKNOWN, WANG_CLIM2_TARGETS_UP, TGCGCANK_UNKNOWN, GOMF_CARBONATE_DEHYDRATASE_ACTIVITY, GGGTGGRR_PAX4_03, CAGCTG_AP4_Q5, AACWWCAANK_UNKNOWN, MODULE_66, FONTAINE_PAPILLARY_THYROID_CARCINOMA_UP, WTGAAAT_UNKNOWN, GNF2_TM4SF2, P300_01, MODULE_295, GOMF_HYDRO_LYASE_ACTIVITY, GRYDER_PAX3FOXO1_ENHANCERS_IN_TADS

GO Biological Process (0):

GO Molecular Function (3): zinc ion binding (GO:0008270), hydro-lyase activity (GO:0016836), carbonate dehydratase activity (GO:0004089)

GO Cellular Component (2): extracellular region (GO:0005576), basolateral plasma membrane (GO:0016323)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transition metal ion binding1
carbon-oxygen lyase activity1
hydro-lyase activity1
cellular anatomical structure1
basal plasma membrane1
plasma membrane region1

Protein interactions and networks

STRING

1124 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CA11ITPR1Q14643453
CA11EVPLLA8MZ36451
CA11SLFNL1Q499Z3449
CA11BSGP35613409
CA11GGTLC1Q9BX51356
CA11REM2Q8IYK8348
CA11REM1O75628347
CA11ABHD1Q96SE0343
CA11SLC4A2P04920316
CA11ATXN3LQ9H3M9316
CA11MCAMP43121296
CA11ATXN3P54252295
CA11CCAR1Q8IX12295
CA11NMRK1Q9NWW6292
CA11CA12O43570287
CA11CA14Q9ULX7287

IntAct

9 interactions, top by confidence:

ABTypeScore
ANTXR1POTEFpsi-mi:“MI:0914”(association)0.530
TAZMANBApsi-mi:“MI:0914”(association)0.350
INSL5LAMA5psi-mi:“MI:0914”(association)0.350
CRPQSOX1psi-mi:“MI:0914”(association)0.350
PDGFRAGXYLT2psi-mi:“MI:0914”(association)0.350
CA11HSPA5psi-mi:“MI:0914”(association)0.350
LCORCA11psi-mi:“MI:0915”(physical association)0.000

BioGRID (16): CA11 (Affinity Capture-MS), BIRC6 (Affinity Capture-MS), PM20D2 (Affinity Capture-MS), CA11 (Affinity Capture-MS), CA11 (Affinity Capture-MS), CA11 (Affinity Capture-MS), CA11 (Affinity Capture-MS), CA11 (Affinity Capture-MS), CA11 (Synthetic Lethality), CA11 (Affinity Capture-RNA), CA11 (Affinity Capture-MS), BIRC6 (Affinity Capture-MS), HSPA5 (Affinity Capture-MS), CA11 (Negative Genetic), CA11 (Negative Genetic)

ESM2 similar proteins: A0JN41, A2VE04, F4HUC4, F4IHR4, F4JIK2, O04846, O43570, O70354, O75493, P08060, P09172, P0DO50, P15101, P18761, P18915, P22748, P23280, P28651, P35219, P48283, P48284, P61215, Q05754, Q10462, Q18932, Q5PPN4, Q5R4U0, Q5R665, Q5TZ24, Q64237, Q64444, Q68CI2, Q6UVY6, Q6ZNA5, Q75N35, Q7TT41, Q865C0, Q866X6, Q866X7, Q8CI85

Diamond homologs: A0A7H0DN92, A0JN41, B8V7P3, O43570, O57211, O70354, O75493, P00915, P00916, P00918, P00919, P00920, P00921, P00922, P04195, P07450, P07451, P07630, P0DSY1, P0DSY2, P14141, P16015, P20508, P23589, P27139, P28651, P35217, P35218, P35219, P43165, P43166, P48282, P61215, P83299, Q18932, Q1LZA1, Q5PPN4, Q5R4U0, Q5R665, Q5S1S4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance31
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1691 predictions. Top by Δscore:

VariantEffectΔscore
19:48639049:TGCAT:Tacceptor_gain1.0000
19:48639050:GCAT:Gacceptor_gain1.0000
19:48639051:CATC:Cacceptor_gain1.0000
19:48639054:C:CCacceptor_gain1.0000
19:48639055:T:Aacceptor_loss1.0000
19:48639059:G:GCacceptor_gain1.0000
19:48639456:TCAT:Tacceptor_gain1.0000
19:48639457:CAT:Cacceptor_gain1.0000
19:48639457:CATC:Cacceptor_gain1.0000
19:48639459:TC:Tacceptor_loss1.0000
19:48639460:C:CCacceptor_gain1.0000
19:48639547:A:ACdonor_gain1.0000
19:48639548:C:CTdonor_gain1.0000
19:48639548:CT:Cdonor_gain1.0000
19:48639753:A:Cdonor_gain1.0000
19:48639759:C:CAdonor_gain1.0000
19:48639762:T:TAdonor_gain1.0000
19:48639786:A:ACdonor_gain1.0000
19:48639787:C:CCdonor_gain1.0000
19:48640090:ACTAC:Adonor_loss1.0000
19:48640092:TA:Tdonor_loss1.0000
19:48640094:C:Adonor_gain1.0000
19:48640094:C:Gdonor_loss1.0000
19:48640276:CGGAG:Cacceptor_gain1.0000
19:48640280:GCTGT:Gacceptor_loss1.0000
19:48640281:C:CCacceptor_gain1.0000
19:48640282:T:Gacceptor_loss1.0000
19:48645336:AGGTT:Adonor_gain1.0000
19:48645340:T:TAdonor_gain1.0000
19:48638141:TCCA:Tacceptor_gain0.9900

AlphaMissense

2120 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:48639362:G:CC246W0.999
19:48640260:G:CN102K0.999
19:48640260:G:TN102K0.999
19:48644505:G:CS69R0.999
19:48644505:G:TS69R0.999
19:48644507:T:GS69R0.999
19:48644526:A:CC62W0.999
19:48644527:C:GC62S0.999
19:48644527:C:TC62Y0.999
19:48644528:A:TC62S0.999
19:48644556:C:AW52C0.999
19:48644556:C:GW52C0.999
19:48639043:A:GL269P0.998
19:48639357:T:AE248V0.998
19:48639363:C:GC246S0.998
19:48639363:C:TC246Y0.998
19:48639364:A:GC246R0.998
19:48639364:A:TC246S0.998
19:48639385:C:AG239C0.998
19:48639385:C:GG239R0.998
19:48640246:A:TV107D0.998
19:48644503:G:TP70H0.998
19:48644528:A:GC62R0.998
19:48644535:C:AW59C0.998
19:48644535:C:GW59C0.998
19:48644537:A:GW59R0.998
19:48644537:A:TW59R0.998
19:48644558:A:GW52R0.998
19:48644558:A:TW52R0.998
19:48638959:C:AR297M0.997

dbSNP variants (sampled 300 via entrez): RS1000296980 (19:48644083 G>T), RS1000364775 (19:48641437 T>A), RS1000649208 (19:48643649 T>A,C,G), RS1001041792 (19:48646156 T>C), RS1001059334 (19:48646448 AG>A,AGG), RS1001542678 (19:48642929 A>G,T), RS1001777111 (19:48644785 G>A,T), RS1002174230 (19:48637741 T>A,C,G), RS1002273151 (19:48641198 T>G), RS1002326164 (19:48645010 CT>C,CTT), RS1002653821 (19:48646581 C>A,G,T), RS1003456931 (19:48647663 A>G,T), RS1003526314 (19:48638652 C>T), RS1003796977 (19:48641558 G>A), RS1003986851 (19:48639090 A>C,G,T)

Disease associations

OMIM: gene MIM:604644 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

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: yes

ChEMBL targets (1): CHEMBL2420 (SINGLE PROTEIN)

Molecules with ChEMBL bioactivity

1 molecules (phase ≥1), by development phase (incl. off-target/promiscuous compounds). Patent mentions across the top 20 by phase: 28,768 (via chembl_molecule»patent_compound — counts attach to the compound, not the gene–compound relationship, so off-target/promiscuous molecules can dominate).

MoleculeNamePhasePatents
CHEMBL20ACETAZOLAMIDE428,768

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

ChEMBL bioactivities

14 potent at pChembl≥5 of 14 total, top 14 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).

pChemblTypeValueUnitMolecule
8.92Ki1.2nMCHEMBL4080604
8.39Ki4.1nMCHEMBL4097126
8.35Ki4.5nMCHEMBL4081547
8.24Ki5.7nMCHEMBL4070963
8.24Ki5.8nMCHEMBL4061260
8.24Ki5.7nMACETAZOLAMIDE
8.23Ki5.9nMCHEMBL4069928
8.22Ki6nMCHEMBL4099555
8.21Ki6.1nMCHEMBL4089415
8.20Ki6.3nMCHEMBL4064015
8.16Ki6.9nMCHEMBL4091812
7.34Ki45.5nMCHEMBL4104834
7.08Ki82.3nMCHEMBL4093328
7.06Ki87.3nMCHEMBL4072614

PubChem BioAssay actives

14 with measured affinity, of 23 total; 14 most potent distinct compounds. Largely complementary to BindingDB; screening values are coarse (µM, 4 dp), so sub-nM hits tie at the floor.

CompoundAssayTypeValueUnit
sodium 2-hydroxy-3-[(4-sulfamoylphenyl)carbamothioyldiazenyl]-1H-indole-5-sulfonate1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0012uM
1-[(2-hydroxy-5-nitro-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0041uM
1-[(5-fluoro-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0045uM
1-[(2-hydroxy-5-methyl-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0057uM
Acetazolamide1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0057uM
1-[(5-chloro-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0058uM
1-[(2-hydroxy-5-iodo-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0059uM
1-[[2-hydroxy-5-(trifluoromethoxy)-1H-indol-3-yl]imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0060uM
1-[(5-bromo-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0061uM
1-[(5,7-dibromo-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0063uM
1-[(2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0069uM
1-[(7-fluoro-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0455uM
1-[(5,7-dichloro-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0823uM
1-[(7-chloro-2-hydroxy-1H-indol-3-yl)imino]-3-(4-sulfamoylphenyl)thiourea1454029: Inhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayki0.0873uM

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects cotreatment, decreases expression, affects expression7
Estradioldecreases expression, increases expression, affects cotreatment3
bisphenol Adecreases methylation, increases expression2
aristolochic acid Iincreases expression1
afuresertibincreases expression1
pirinixic acidaffects binding, increases activity, increases expression1
terbufosdecreases methylation1
trichostatin Adecreases expression1
mono-(2-ethylhexyl)phthalatedecreases expression1
sodium arsenitedecreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphinaffects cotreatment, decreases expression1
bisphenol Sincreases expression1
bis-N,N-dimethylamino-2-(N-methylpyrrolyl)methyl cyclopentadienyl titanium (IV)increases expression1
(+)-JQ1 compounddecreases expression1
Fulvestrantdecreases methylation1
Air Pollutantsdecreases expression, increases abundance1
Carbamazepineaffects expression1
Cisplatindecreases expression1
Doxorubicindecreases expression1
Fonofosdecreases methylation1
Oxygenincreases expression1
Parathiondecreases methylation1
Silicon Dioxidedecreases expression1
Tetrachlorodibenzodioxinaffects cotreatment, decreases expression1
Tretinoindecreases expression1
Triclosanincreases expression1
Okadaic Aciddecreases expression1
Particulate Matterdecreases expression, increases abundance1

ChEMBL screening assays

2 unique, capped per target: 2 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL4036367BindingInhibition of recombinant human membrane bound carbonic anhydrase 11 expressed in Escherichia coli pretreated for 15 mins prior to testing by stopped-flow assayNovel sulfonamide-containing 2-indolinones that selectively inhibit tumor-associated alpha carbonic anhydrases. — Bioorg Med Chem

Clinical trials (associated diseases)

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.