CORO2B
gene geneOn this page
Also known as ClipinCKIAA0925
Summary
CORO2B (coronin 2B, HGNC:2256) is a protein-coding gene on chromosome 15q23, encoding Coronin-2B (Q9UQ03). May play a role in the reorganization of neuronal actin structure.
Enables talin binding activity and vinculin binding activity. Acts upstream of or within several processes, including negative regulation of cell-substrate adhesion; regulation of actin cytoskeleton organization; and regulation of establishment of protein localization. Located in focal adhesion.
Source: NCBI Gene 10391 — RefSeq curated summary.
At a glance
- GWAS associations: 4
- Clinical variants (ClinVar): 68 total
- MANE Select transcript:
NM_006091
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:2256 |
| Approved symbol | CORO2B |
| Name | coronin 2B |
| Location | 15q23 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | ClipinC, KIAA0925 |
| Ensembl gene | ENSG00000103647 |
| Ensembl biotype | protein_coding |
| OMIM | 605002 |
| Entrez | 10391 |
Gene structure
Transcript identifiers
Ensembl transcripts: 5 — 5 protein_coding
ENST00000261861, ENST00000540068, ENST00000543950, ENST00000972054, ENST00000972055
RefSeq mRNA: 5 — MANE Select: NM_006091
NM_001190456, NM_001190457, NM_001324014, NM_001324015, NM_006091
CCDS: CCDS10229, CCDS53952
Canonical transcript exons
ENST00000261861 — 12 exons
| Exon | Start | End |
|---|---|---|
| ENSE00000449772 | 68695140 | 68695256 |
| ENSE00000696033 | 68714559 | 68714663 |
| ENSE00000696037 | 68713925 | 68714041 |
| ENSE00000696042 | 68711542 | 68711706 |
| ENSE00000696046 | 68710732 | 68710881 |
| ENSE00001027034 | 68719144 | 68719234 |
| ENSE00001027050 | 68719413 | 68719552 |
| ENSE00001027055 | 68715215 | 68715311 |
| ENSE00001251788 | 68718698 | 68718810 |
| ENSE00001405057 | 68578993 | 68579277 |
| ENSE00001550990 | 68725843 | 68727806 |
| ENSE00003758263 | 68645160 | 68645360 |
Expression profiles
Bgee: expression breadth ubiquitous, 229 present calls, max score 97.79.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 19.2836 / max 548.2872, expressed in 1257 samples.
FANTOM5 promoters (12 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 147405 | 5.5540 | 978 |
| 147409 | 5.2323 | 1016 |
| 147410 | 5.1006 | 952 |
| 147403 | 0.6612 | 341 |
| 147408 | 0.6351 | 216 |
| 147404 | 0.5464 | 306 |
| 147413 | 0.4523 | 150 |
| 147407 | 0.3886 | 157 |
| 147412 | 0.2735 | 91 |
| 147406 | 0.2714 | 117 |
Top tissues by expression
295 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| ganglionic eminence | UBERON:0004023 | 97.79 | gold quality |
| middle frontal gyrus | UBERON:0002702 | 97.19 | gold quality |
| Brodmann (1909) area 10 | UBERON:0013541 | 96.52 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 96.40 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 96.28 | gold quality |
| inferior olivary complex | UBERON:0002127 | 96.27 | gold quality |
| Brodmann (1909) area 46 | UBERON:0006483 | 96.16 | gold quality |
| prefrontal cortex | UBERON:0000451 | 96.08 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 95.95 | gold quality |
| cerebellar cortex | UBERON:0002129 | 95.94 | gold quality |
| spinal cord | UBERON:0002240 | 95.93 | gold quality |
| caudate nucleus | UBERON:0001873 | 95.91 | gold quality |
| postcentral gyrus | UBERON:0002581 | 95.87 | gold quality |
| CA1 field of hippocampus | UBERON:0003881 | 95.85 | gold quality |
| inferior vagus X ganglion | UBERON:0005363 | 95.80 | gold quality |
| parietal lobe | UBERON:0001872 | 95.70 | gold quality |
| lateral nuclear group of thalamus | UBERON:0002736 | 95.68 | gold quality |
| cerebellum | UBERON:0002037 | 95.67 | gold quality |
| right frontal lobe | UBERON:0002810 | 95.58 | gold quality |
| cortical plate | UBERON:0005343 | 95.54 | gold quality |
| putamen | UBERON:0001874 | 95.36 | gold quality |
| nucleus accumbens | UBERON:0001882 | 95.36 | gold quality |
| dorsal motor nucleus of vagus nerve | UBERON:0002870 | 95.36 | gold quality |
| frontal pole | UBERON:0002795 | 95.24 | gold quality |
| frontal cortex | UBERON:0001870 | 95.22 | gold quality |
| subthalamic nucleus | UBERON:0001906 | 95.21 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 95.05 | gold quality |
| neocortex | UBERON:0001950 | 94.85 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 94.79 | gold quality |
| paraflocculus | UBERON:0005351 | 94.78 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 6.25 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
163 targeting CORO2B, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-4747-5P | 100.00 | 67.90 | 2681 |
| HSA-MIR-5196-5P | 100.00 | 67.98 | 2761 |
| HSA-MIR-1252-5P | 100.00 | 69.80 | 2774 |
| HSA-MIR-12118 | 100.00 | 65.88 | 1270 |
| HSA-MIR-4533 | 100.00 | 69.48 | 2758 |
| HSA-MIR-5692A | 100.00 | 74.40 | 6850 |
| HSA-MIR-4534 | 99.99 | 66.58 | 1907 |
| HSA-MIR-6077 | 99.99 | 68.04 | 2299 |
| HSA-MIR-103A-3P | 99.98 | 69.14 | 1595 |
| HSA-MIR-107 | 99.98 | 69.14 | 1595 |
| HSA-MIR-3173-3P | 99.98 | 66.49 | 1217 |
| HSA-MIR-6891-5P | 99.98 | 66.53 | 1372 |
| HSA-MIR-3148 | 99.97 | 75.06 | 6478 |
| HSA-MIR-6888-3P | 99.97 | 65.95 | 1170 |
| HSA-MIR-7152-3P | 99.97 | 67.47 | 849 |
| HSA-MIR-4725-3P | 99.96 | 69.53 | 2520 |
| HSA-MIR-6780B-5P | 99.96 | 69.60 | 2562 |
| HSA-MIR-570-3P | 99.96 | 72.41 | 4910 |
| HSA-MIR-302E | 99.96 | 70.74 | 2669 |
| HSA-MIR-2110 | 99.96 | 66.68 | 1930 |
| HSA-MIR-185-3P | 99.95 | 67.01 | 1743 |
| HSA-MIR-8082 | 99.95 | 67.27 | 1170 |
| HSA-MIR-651-3P | 99.94 | 73.48 | 5177 |
| HSA-MIR-145-5P | 99.92 | 71.13 | 1836 |
| HSA-MIR-5195-3P | 99.92 | 70.92 | 1877 |
| HSA-MIR-106A-5P | 99.90 | 73.94 | 2683 |
| HSA-MIR-4731-5P | 99.89 | 67.23 | 2537 |
| HSA-MIR-345-3P | 99.89 | 70.23 | 1421 |
| HSA-MIR-17-5P | 99.89 | 73.83 | 2665 |
| HSA-MIR-302A-3P | 99.89 | 71.23 | 1777 |
Literature-anchored findings (GeneRIF, showing 2)
- CORO2B is a novel podocyte enriched protein influencing cytoskeletal plasticity and stress adaptation. (PMID:29162887)
- Coro2b, a podocyte protein downregulated in human diabetic nephropathy, is involved in the development of protamine sulphate-induced foot process effacement. (PMID:31221975)
Cross-species orthologs
6 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | coro2bb | ENSDARG00000063604 |
| danio_rerio | coro2ba | ENSDARG00000079440 |
| mus_musculus | Coro2b | ENSMUSG00000041729 |
| rattus_norvegicus | Coro2b | ENSRNOG00000015257 |
| drosophila_melanogaster | coro | FBGN0265935 |
| caenorhabditis_elegans | WBGENE00000768 |
Paralogs (6): CORO1A (ENSG00000102879), CORO2A (ENSG00000106789), CORO1C (ENSG00000110880), CORO6 (ENSG00000167549), CORO1B (ENSG00000172725), CORO7 (ENSG00000262246)
Protein
Protein identifiers
Coronin-2B — Q9UQ03 (reviewed: Q9UQ03)
Alternative names: Coronin-like protein C, Protein FC96
All UniProt accessions (1): Q9UQ03
UniProt curated annotations — full annotation on UniProt →
Function. May play a role in the reorganization of neuronal actin structure.
Subunit / interactions. Binds to F-actin and to vinculin.
Subcellular location. Cytoplasm. Cytoskeleton.
Tissue specificity. Expressed predominantly in brain.
Similarity. Belongs to the WD repeat coronin family.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q9UQ03-1 | 1 | yes |
| Q9UQ03-2 | 2 |
RefSeq proteins (5): NP_001177385, NP_001177386, NP_001310943, NP_001310944, NP_006082* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR001680 | WD40_rpt | Repeat |
| IPR015048 | DUF1899 | Domain |
| IPR015505 | Coronin | Family |
| IPR015943 | WD40/YVTN_repeat-like_dom_sf | Homologous_superfamily |
| IPR019775 | WD40_repeat_CS | Conserved_site |
| IPR036322 | WD40_repeat_dom_sf | Homologous_superfamily |
Pfam: PF00400, PF08953, PF16300
UniProt features (13 total): repeat 7, sequence variant 2, chain 1, sequence conflict 1, coiled-coil region 1, splice variant 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9UQ03-F1 | 91.58 | 0.80 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 255 (showing top):
GOBP_ACTIN_FILAMENT_BUNDLE_ORGANIZATION, GOBP_REGULATION_OF_BLOOD_PRESSURE, GOBP_CIRCULATORY_SYSTEM_PROCESS, GOBP_RENAL_SYSTEM_PROCESS_INVOLVED_IN_REGULATION_OF_BLOOD_VOLUME, GOBP_FOCAL_ADHESION_ASSEMBLY, GOBP_REGULATION_OF_SYSTEMIC_ARTERIAL_BLOOD_PRESSURE, GOBP_REGULATION_OF_CELLULAR_COMPONENT_BIOGENESIS, CAGCTG_AP4_Q5, GOBP_REGULATION_OF_GLOMERULAR_FILTRATION, GOBP_NEGATIVE_REGULATION_OF_CELLULAR_COMPONENT_ORGANIZATION, GOBP_REGULATION_OF_ACTIN_FILAMENT_BASED_PROCESS, GOBP_NEGATIVE_REGULATION_OF_CELL_SUBSTRATE_ADHESION, GOBP_CELL_JUNCTION_ORGANIZATION, GOBP_NEGATIVE_REGULATION_OF_ACTIN_FILAMENT_BUNDLE_ASSEMBLY, GOBP_ACTIN_FILAMENT_ORGANIZATION
GO Biological Process (9): regulation of glomerular filtration (GO:0003093), negative regulation of cell-substrate adhesion (GO:0010812), actin cytoskeleton organization (GO:0030036), regulation of actin cytoskeleton organization (GO:0032956), focal adhesion assembly (GO:0048041), negative regulation of stress fiber assembly (GO:0051497), regulation of cellular response to stress (GO:0080135), negative regulation of establishment of protein localization (GO:1904950), positive regulation of establishment of protein localization (GO:1904951)
GO Molecular Function (5): actin binding (GO:0003779), vinculin binding (GO:0017166), actin filament binding (GO:0051015), talin binding (GO:1990147), protein binding (GO:0005515)
GO Cellular Component (5): focal adhesion (GO:0005925), actin cytoskeleton (GO:0015629), membrane (GO:0016020), cytoplasm (GO:0005737), cytoskeleton (GO:0005856)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cytoskeletal protein binding | 3 |
| establishment of protein localization | 2 |
| regulation of establishment of protein localization | 2 |
| cellular anatomical structure | 2 |
| glomerular filtration | 1 |
| regulation of renal system process | 1 |
| negative regulation of cell adhesion | 1 |
| regulation of cell-substrate adhesion | 1 |
| cell-substrate adhesion | 1 |
| cytoskeleton organization | 1 |
| actin filament-based process | 1 |
| actin cytoskeleton organization | 1 |
| regulation of actin filament-based process | 1 |
| regulation of cytoskeleton organization | 1 |
| cell-substrate junction assembly | 1 |
| cell-matrix adhesion | 1 |
| negative regulation of actin filament bundle assembly | 1 |
| stress fiber assembly | 1 |
| regulation of stress fiber assembly | 1 |
| cellular response to stress | 1 |
| regulation of cellular process | 1 |
| regulation of response to stress | 1 |
| negative regulation of biological process | 1 |
| positive regulation of biological process | 1 |
| actin binding | 1 |
| protein-containing complex binding | 1 |
| binding | 1 |
| cell-substrate junction | 1 |
| cytoskeleton | 1 |
| intracellular anatomical structure | 1 |
| intracellular membraneless organelle | 1 |
Protein interactions and networks
STRING
2200 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| CORO2B | ITGA11 | Q9UKX5 | 834 |
| CORO2B | TLE3 | Q04726 | 810 |
| CORO2B | KIF23 | Q02241 | 663 |
| CORO2B | VCL | P18206 | 549 |
| CORO2B | ZNF567 | Q8N184 | 327 |
| CORO2B | SYCE1L | A8MT33 | 321 |
| CORO2B | RELL1 | Q8IUW5 | 321 |
| CORO2B | URB2 | Q14146 | 317 |
| CORO2B | CDV3 | Q9UKY7 | 317 |
| CORO2B | RABEPK | Q7Z6M1 | 316 |
| CORO2B | ANKRD34B | A5PLL1 | 310 |
| CORO2B | CDH24 | Q86UP0 | 307 |
| CORO2B | KLHL24 | Q6TFL4 | 302 |
| CORO2B | ZNF768 | Q9H5H4 | 301 |
| CORO2B | SS18L2 | Q9UHA2 | 301 |
IntAct
41 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| APPBP2 | CORO2B | psi-mi:“MI:0915”(physical association) | 0.720 |
| CORO2B | APPBP2 | psi-mi:“MI:0915”(physical association) | 0.720 |
| DBN1 | SVIL | psi-mi:“MI:0914”(association) | 0.530 |
| SSH1 | GSN | psi-mi:“MI:0914”(association) | 0.530 |
| CORO2A | BCLAF1 | psi-mi:“MI:0914”(association) | 0.500 |
| CORO2B | psi-mi:“MI:0915”(physical association) | 0.400 | |
| NUDC | CORO2B | psi-mi:“MI:0915”(physical association) | 0.400 |
| P | psi-mi:“MI:0914”(association) | 0.350 | |
| CTBP1 | TAF15 | psi-mi:“MI:0914”(association) | 0.350 |
| DAPK1 | MYO1C | psi-mi:“MI:0914”(association) | 0.350 |
| MAPT | SHTN1 | psi-mi:“MI:0914”(association) | 0.350 |
| CEP63 | CIBAR1 | psi-mi:“MI:0914”(association) | 0.350 |
| ANK2 | IGKV2-40 | psi-mi:“MI:0914”(association) | 0.350 |
| DYRK1A | TEX13D | psi-mi:“MI:0914”(association) | 0.350 |
| ITM2B | ILVBL | psi-mi:“MI:0914”(association) | 0.350 |
| SYNGAP1 | POTEF | psi-mi:“MI:0914”(association) | 0.350 |
| HCN1 | POTEF | psi-mi:“MI:0914”(association) | 0.350 |
| CORO2B | SHC1 | psi-mi:“MI:0914”(association) | 0.350 |
| CORO2A | YPEL5 | psi-mi:“MI:0914”(association) | 0.350 |
| CORO2B | OBI1 | psi-mi:“MI:0914”(association) | 0.350 |
| VCP | SHTN1 | psi-mi:“MI:0914”(association) | 0.350 |
| VCP | FAM171A2 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (30): APPBP2 (Two-hybrid), CORO2A (Affinity Capture-MS), PRKG1 (Affinity Capture-MS), SHC1 (Affinity Capture-MS), ARHGEF25 (Affinity Capture-MS), CORO2B (Two-hybrid), CORO2B (Two-hybrid), CORO2B (Affinity Capture-Western), CORO2B (Negative Genetic), CORO2B (Affinity Capture-MS), SHC1 (Affinity Capture-MS), CORO2A (Affinity Capture-MS), ARHGEF25 (Affinity Capture-MS), PRKG1 (Affinity Capture-MS), CORO2B (Affinity Capture-MS)
ESM2 similar proteins: A0A286ZK88, A1L1L6, A7MB28, A8WGF4, B8BJ39, D0G6S1, O00399, O54956, P11029, P11497, Q13085, Q148G7, Q28007, Q28943, Q28DR7, Q2HJF8, Q2RAK2, Q4R4U1, Q502J7, Q5FVD6, Q5R559, Q5R5F8, Q5R7D8, Q5R8Q7, Q5SWU9, Q5ZIT8, Q5ZM73, Q6AYR2, Q6NVC5, Q6NWV3, Q6P1X5, Q6PC62, Q7TPD1, Q7TSL3, Q86XK2, Q8BG51, Q8BH44, Q8C176, Q8CHR6, Q8IWZ6
Diamond homologs: A8WGE3, B0R0D7, O13923, O89046, O89053, P27133, P31146, P57737, Q06440, Q21624, Q32LP9, Q4R4J2, Q54JS5, Q5NVK4, Q6DJD8, Q6QEF8, Q7K0L4, Q8BH44, Q8C0P5, Q91ZN1, Q920J3, Q920M5, Q92176, Q92828, Q9BR76, Q9ULV4, Q9UQ03, Q9WUM3, Q9WUM4, Q9XS70, A6ZPA9, A7TMF9, B3RNR8, B6QC56, B8N9H4, C5FWH1, C7Z6H2, F1LTR1, G0S8H7, O13637
SIGNOR signaling
0 interactions.
Enriched among interaction partners
Reactome pathways and GO biological processes over-represented among this gene’s 40 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 |
|---|---|---|---|
| actin filament organization | 5 | 16.9× | 4e-03 |
Disease & clinical
Clinical variants and AI predictions
ClinVar
68 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 57 |
| Likely benign | 3 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
2684 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 15:68579275:AAGG:A | donor_loss | 1.0000 |
| 15:68579278:G:GA | donor_loss | 1.0000 |
| 15:68579279:T:A | donor_loss | 1.0000 |
| 15:68645157:C:G | acceptor_gain | 1.0000 |
| 15:68645158:A:AG | acceptor_gain | 1.0000 |
| 15:68645159:G:GA | acceptor_gain | 1.0000 |
| 15:68645159:GA:G | acceptor_gain | 1.0000 |
| 15:68645159:GAT:G | acceptor_gain | 1.0000 |
| 15:68645357:GCAG:G | donor_gain | 1.0000 |
| 15:68645358:CAGG:C | donor_loss | 1.0000 |
| 15:68645361:G:GG | donor_gain | 1.0000 |
| 15:68695135:T:TA | acceptor_gain | 1.0000 |
| 15:68695137:CA:C | acceptor_loss | 1.0000 |
| 15:68695138:A:AG | acceptor_gain | 1.0000 |
| 15:68695138:A:G | acceptor_loss | 1.0000 |
| 15:68695139:G:GG | acceptor_gain | 1.0000 |
| 15:68695139:GA:G | acceptor_gain | 1.0000 |
| 15:68695139:GAC:G | acceptor_gain | 1.0000 |
| 15:68695139:GACA:G | acceptor_gain | 1.0000 |
| 15:68695253:GTCG:G | donor_gain | 1.0000 |
| 15:68695254:TCG:T | donor_gain | 1.0000 |
| 15:68695257:G:GG | donor_gain | 1.0000 |
| 15:68695257:GTGAG:G | donor_loss | 1.0000 |
| 15:68695259:GAGCA:G | donor_loss | 1.0000 |
| 15:68710727:TGCAG:T | acceptor_loss | 1.0000 |
| 15:68710728:GCAGG:G | acceptor_loss | 1.0000 |
| 15:68710729:CAGG:C | acceptor_loss | 1.0000 |
| 15:68710730:A:AC | acceptor_loss | 1.0000 |
| 15:68710731:G:A | acceptor_loss | 1.0000 |
| 15:68710880:AG:A | donor_gain | 1.0000 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000010858 (15:68598844 G>A), RS1000025885 (15:68706707 ATTTT>A,ATTT,ATTTTT), RS1000076671 (15:68595192 T>G), RS1000077004 (15:68579669 G>C), RS1000079689 (15:68634805 C>T), RS1000081488 (15:68545137 G>A,C,T), RS1000084095 (15:68599045 G>A), RS1000108536 (15:68538478 T>A,C), RS1000115203 (15:68704794 G>A,C), RS1000132554 (15:68550943 T>A), RS1000141270 (15:68552967 A>G), RS1000155167 (15:68720915 C>T), RS1000161985 (15:68717132 T>A,C), RS1000166404 (15:68659529 A>G), RS1000169890 (15:68589757 C>T)
Disease associations
OMIM: gene MIM:605002 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
4 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST000477_44 | Cognitive performance | 1.000000e-07 |
| GCST003670_1 | Systolic blood pressure | 3.000000e-08 |
| GCST010320_28 | PR interval | 8.000000e-09 |
| GCST010321_45 | PR interval | 1.000000e-08 |
EFO canonical traits (3, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0003926 | neuropsychological test |
| EFO:0006335 | systolic blood pressure |
| EFO:0004462 | PR interval |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
48 total (human), top 30 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Benzo(a)pyrene | affects methylation, decreases expression | 3 |
| bisphenol A | affects cotreatment, increases expression, decreases methylation | 2 |
| Tretinoin | increases expression | 2 |
| Cyclosporine | increases expression | 2 |
| FR900359 | increases phosphorylation | 1 |
| bisphenol F | affects cotreatment, increases methylation | 1 |
| deoxynivalenol | decreases expression | 1 |
| sodium arsenate | decreases expression | 1 |
| tris(2-butoxyethyl) phosphate | affects expression | 1 |
| sodium arsenite | increases expression | 1 |
| butyraldehyde | increases expression | 1 |
| benzo(e)pyrene | increases methylation | 1 |
| potassium chromate(VI) | decreases expression | 1 |
| aflatoxin B2 | decreases methylation | 1 |
| nickel sulfate | decreases expression | 1 |
| S-(1,2-dichlorovinyl)cysteine | affects cotreatment, decreases expression | 1 |
| diallyl trisulfide | increases expression | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| 2,2’,4,4’,5-brominated diphenyl ether | increases expression | 1 |
| clothianidin | decreases expression | 1 |
| jinfukang | affects cotreatment, decreases expression | 1 |
| Sunitinib | decreases expression | 1 |
| Fulvestrant | affects cotreatment, increases methylation | 1 |
| Vorinostat | decreases expression | 1 |
| Cisplatin | affects cotreatment, decreases expression | 1 |
| Dexamethasone | affects cotreatment, increases expression | 1 |
| Endosulfan | increases expression | 1 |
| Estradiol | affects cotreatment, increases expression | 1 |
| Indomethacin | affects cotreatment, increases expression | 1 |
| Lipopolysaccharides | affects cotreatment, decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.