CD302
gene geneOn this page
Also known as DCL-1KIAA0022BIMLECCLEC13A
Summary
CD302 (CD302 molecule, HGNC:30843) is a protein-coding gene on chromosome 2q24.2, encoding CD302 antigen (Q8IX05). Multifunctional C-type lectin receptor involved in endocytosis, phagocytosis and regulation of cell adhesion and migration.
CD302 is a C-type lectin receptor involved in cell adhesion and migration, as well as endocytosis and phagocytosis (Kato et al., 2007 [PubMed 17947679]).
Source: NCBI Gene 9936 — RefSeq curated summary.
At a glance
- GWAS associations: 3
- Clinical variants (ClinVar): 10 total
- MANE Select transcript:
NM_014880
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:30843 |
| Approved symbol | CD302 |
| Name | CD302 molecule |
| Location | 2q24.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | DCL-1, KIAA0022, BIMLEC, CLEC13A |
| Ensembl gene | ENSG00000241399 |
| Ensembl biotype | protein_coding |
| OMIM | 612246 |
| Entrez | 9936 |
Gene structure
Transcript identifiers
Ensembl transcripts: 13 — 12 protein_coding, 1 protein_coding_CDS_not_defined
ENST00000259053, ENST00000429078, ENST00000480212, ENST00000553424, ENST00000856855, ENST00000856856, ENST00000856857, ENST00000856858, ENST00000856859, ENST00000856860, ENST00000856861, ENST00000966882, ENST00000966883
RefSeq mRNA: 3 — MANE Select: NM_014880
NM_001198763, NM_001198764, NM_014880
CCDS: CCDS33308, CCDS56139, CCDS74595
Canonical transcript exons
ENST00000259053 — 6 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003482872 | 159783359 | 159783469 |
| ENSE00003560104 | 159768628 | 159772053 |
| ENSE00003657339 | 159798132 | 159798208 |
| ENSE00003730131 | 159777938 | 159777964 |
| ENSE00003735029 | 159780005 | 159780178 |
| ENSE00003743188 | 159780882 | 159780998 |
Expression profiles
Bgee: expression breadth ubiquitous, 279 present calls, max score 97.76.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 23.8494 / max 627.3352, expressed in 1477 samples.
FANTOM5 promoters (3 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 31454 | 18.7221 | 1411 |
| 31455 | 4.9253 | 1131 |
| 31456 | 0.2020 | 85 |
Top tissues by expression
294 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| lower lobe of lung | UBERON:0008949 | 97.76 | gold quality |
| monocyte | CL:0000576 | 97.72 | gold quality |
| mononuclear cell | CL:0000842 | 97.71 | gold quality |
| leukocyte | CL:0000738 | 97.35 | gold quality |
| right lung | UBERON:0002167 | 97.02 | gold quality |
| liver | UBERON:0002107 | 96.54 | gold quality |
| synovial joint | UBERON:0002217 | 96.24 | gold quality |
| trabecular bone tissue | UBERON:0002483 | 96.21 | gold quality |
| layer of synovial tissue | UBERON:0007616 | 95.57 | gold quality |
| right lobe of liver | UBERON:0001114 | 95.37 | gold quality |
| calcaneal tendon | UBERON:0003701 | 95.34 | gold quality |
| superficial temporal artery | UBERON:0001614 | 95.31 | gold quality |
| urethra | UBERON:0000057 | 95.22 | gold quality |
| mammary duct | UBERON:0001765 | 94.99 | gold quality |
| skin of hip | UBERON:0001554 | 94.80 | gold quality |
| right coronary artery | UBERON:0001625 | 94.20 | gold quality |
| decidua | UBERON:0002450 | 93.98 | gold quality |
| pericardium | UBERON:0002407 | 93.95 | gold quality |
| epithelium of mammary gland | UBERON:0003244 | 93.88 | gold quality |
| jejunal mucosa | UBERON:0000399 | 93.65 | gold quality |
| lung | UBERON:0002048 | 93.53 | gold quality |
| pigmented layer of retina | UBERON:0001782 | 93.52 | gold quality |
| blood vessel layer | UBERON:0004797 | 93.46 | gold quality |
| thoracic mammary gland | UBERON:0005200 | 93.44 | gold quality |
| pleura | UBERON:0000977 | 93.32 | gold quality |
| mammary gland | UBERON:0001911 | 93.24 | gold quality |
| parietal pleura | UBERON:0002400 | 93.24 | gold quality |
| visceral pleura | UBERON:0002401 | 93.24 | gold quality |
| adipose tissue | UBERON:0001013 | 93.08 | gold quality |
| gall bladder | UBERON:0002110 | 93.06 | gold quality |
Single-cell (SCXA)
Detected in 8 experiment(s), a significant marker in 8.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-CURD-46 | yes | 33.68 |
| E-MTAB-9221 | yes | 28.53 |
| E-GEOD-134144 | yes | 26.30 |
| E-HCAD-10 | yes | 26.04 |
| E-CURD-112 | yes | 24.96 |
| E-CURD-88 | yes | 20.61 |
| E-ANND-3 | yes | 14.37 |
| E-MTAB-9467 | yes | 11.66 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
149 targeting CD302, 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-5011-5P | 100.00 | 83.46 | 5820 |
| HSA-MIR-3163 | 100.00 | 77.23 | 8605 |
| HSA-MIR-4262 | 100.00 | 73.26 | 3931 |
| HSA-MIR-1252-5P | 100.00 | 69.80 | 2774 |
| HSA-MIR-340-5P | 100.00 | 72.50 | 4437 |
| HSA-MIR-190A-3P | 100.00 | 80.35 | 5520 |
| HSA-MIR-5692B | 100.00 | 71.32 | 2622 |
| HSA-MIR-5692C | 100.00 | 71.32 | 2622 |
| HSA-MIR-6867-5P | 100.00 | 82.21 | 3464 |
| HSA-MIR-518D-5P | 100.00 | 67.51 | 979 |
| HSA-MIR-518E-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-518F-5P | 100.00 | 67.51 | 979 |
| HSA-MIR-519A-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-519B-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-519C-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-520C-5P | 100.00 | 67.51 | 979 |
| HSA-MIR-522-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-523-5P | 100.00 | 67.66 | 954 |
| HSA-MIR-526A-5P | 100.00 | 67.51 | 979 |
| HSA-MIR-513A-5P | 100.00 | 69.77 | 2465 |
| HSA-MIR-1277-5P | 100.00 | 73.95 | 5056 |
| HSA-MIR-4282 | 99.99 | 75.36 | 6408 |
| HSA-MIR-181A-5P | 99.99 | 72.96 | 2995 |
| HSA-MIR-181B-5P | 99.99 | 72.97 | 2996 |
| HSA-MIR-181C-5P | 99.99 | 72.95 | 2996 |
| HSA-MIR-181D-5P | 99.99 | 73.04 | 2997 |
| HSA-MIR-520G-5P | 99.99 | 66.76 | 658 |
| HSA-MIR-186-5P | 99.99 | 70.83 | 3707 |
| HSA-MIR-548P | 99.98 | 72.25 | 3784 |
| HSA-MIR-548N | 99.98 | 71.94 | 4170 |
Literature-anchored findings (GeneRIF, showing 6)
- Hodgkin’s lymphoma cell lines express a fusion protein encoded by intergenically spliced mRNA for the multilectin receptor DEC-205 (CD205) and a novel C-type lectin receptor DCL-1 (PMID:12824192)
- hDCL-1 is an unconventional lectin receptor that plays roles not only in endocytosis/phagocytosis but also in cell adhesion and migration (PMID:17947679)
- DLC1 equilibrium unfolding is characterized at the amino acid level. (PMID:19317456)
- These studies confirm a functional role for CD302 in myeloid dendritic cells migration. (PMID:27316686)
- Particle Morphology of Medusavirus Inside and Outside the Cells Reveals a New Maturation Process of Giant Viruses. (PMID:35297671)
- The Human Liver-Expressed Lectin CD302 Restricts Hepatitis C Virus Infection. (PMID:35297672)
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | cd302 | ENSDARG00000086100 |
| mus_musculus | Cd302 | ENSMUSG00000060703 |
| rattus_norvegicus | Cd302 | ENSRNOG00000006623 |
| caenorhabditis_elegans | WBGENE00010228 |
Paralogs (4): MRC2 (ENSG00000011028), LY75 (ENSG00000054219), PLA2R1 (ENSG00000153246), MRC1 (ENSG00000260314)
Protein
Protein identifiers
CD302 antigen — Q8IX05 (reviewed: Q8IX05)
Alternative names: C-type lectin BIMLEC, C-type lectin domain family 13 member A, DEC205-associated C-type lectin 1, Type I transmembrane C-type lectin receptor DCL-1
All UniProt accessions (2): Q8IX05, A0A087WT00
UniProt curated annotations — full annotation on UniProt →
Function. Multifunctional C-type lectin receptor involved in endocytosis, phagocytosis and regulation of cell adhesion and migration. Plays a critical role in guiding dendritic cells to lymph nodes. Also functions as a restriction factor for Hepatitis C virus (HCV) at the liver cell surface, likely by inhibiting a viral cell entry step.
Subcellular location. Cell membrane. Cell projection. Filopodium. Cytoplasm. Cell cortex. Microvillus.
Tissue specificity. Expressed at moderate levels in monocytes, myeloid blood dendritic cells and granulocytes and at low levels in plasmacytoid blood dendritic cells, monocyte-derived macrophages and monocyte-derived dendritic cells, with no expression detected in T-lymphocytes, B-lymphocytes and natural killer cells (at protein level). Expressed widely in different tissues, with highest expression levels in liver, lung, peripheral blood leukocytes and spleen, and lowest levels in neuronal tissues, skeletal muscle and ovary. Isoform 2 and isoform 3 are expressed in malignant Hodgkin lymphoma cells called Hodgkin and Reed-Sternberg (HRS) cells.
Post-translational modifications. May be heterogeneously N-glycosylated in some cell types.
Miscellaneous. Isoform 2 and isoform 3 are produced in HRS cells by a transcriptional control mechanism which cotranscribe an mRNA containing LY75 and CD302 prior to generating the intergenically spliced mRNA to produce LY75/CD302 fusion proteins. Produced by intergenic splicing of LY75 and CD302.
Isoforms (5)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q8IX05-1 | 1 | yes |
| O60449-1 | 4 | |
| Q8IX05-2 | 5 | |
| O60449-2 | 2, Fusion protein variant V34-2 | |
| O60449-3 | 3, Fusion protein variant V33-2 |
RefSeq proteins (3): NP_001185692, NP_001185693, NP_055695* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR001304 | C-type_lectin-like | Domain |
| IPR016186 | C-type_lectin-like/link_sf | Homologous_superfamily |
| IPR016187 | CTDL_fold | Homologous_superfamily |
| IPR050111 | C-type_lectin/snaclec_domain | Family |
Pfam: PF00059
UniProt features (25 total): strand 8, turn 3, helix 2, topological domain 2, splice variant 2, signal peptide 1, chain 1, sequence variant 1, sequence conflict 1, transmembrane region 1, domain 1, glycosylation site 1, disulfide bond 1
Structure
Experimental structures (PDB)
1 structures.
| PDB | Method | Resolution (Å) |
|---|---|---|
| 2NAN | SOLUTION NMR |
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q8IX05-F1 | 80.53 | 0.50 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Disulfide bonds (1): 128–143
Glycosylation sites (1): 109
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 215 (showing top):
BUYTAERT_PHOTODYNAMIC_THERAPY_STRESS_DN, MODULE_45, GOBP_VESICLE_MEDIATED_TRANSPORT, LINDGREN_BLADDER_CANCER_CLUSTER_2A_DN, GNF2_MCL1, GNF2_CD1D, KOYAMA_SEMA3B_TARGETS_UP, HOSHIDA_LIVER_CANCER_SUBCLASS_S3, chr2q24, SANSOM_APC_TARGETS_DN, GNF2_HCK, BASAKI_YBX1_TARGETS_DN, VECCHI_GASTRIC_CANCER_EARLY_DN, GOBP_IMPORT_INTO_CELL, RIGGINS_TAMOXIFEN_RESISTANCE_DN
GO Biological Process (1): phagocytosis (GO:0006909)
GO Molecular Function (3): carbohydrate binding (GO:0030246), signaling receptor activity (GO:0038023), protein binding (GO:0005515)
GO Cellular Component (6): microvillus (GO:0005902), cell cortex (GO:0005938), membrane (GO:0016020), filopodium (GO:0030175), cytoplasm (GO:0005737), cell projection (GO:0042995)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cellular anatomical structure | 3 |
| binding | 2 |
| actin-based cell projection | 2 |
| endocytosis | 1 |
| molecular transducer activity | 1 |
| actin filament bundle | 1 |
| cytoplasm | 1 |
| cell periphery | 1 |
| intracellular anatomical structure | 1 |
Protein interactions and networks
STRING
612 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| CD302 | AGO1 | Q9UL18 | 785 |
| CD302 | DICER1 | Q9UPY3 | 723 |
| CD302 | SRRT | Q9BXP5 | 670 |
| CD302 | MILR1 | Q7Z6M3 | 571 |
| CD302 | DROSHA | Q9NRR4 | 546 |
| CD302 | PIWIL4 | Q7Z3Z4 | 512 |
| CD302 | AGO4 | Q9HCK5 | 510 |
| CD302 | PIWIL1 | Q96J94 | 507 |
| CD302 | LY75 | O60449 | 500 |
| CD302 | SNRPD3 | P43331 | 443 |
| CD302 | AGO2 | Q9UKV8 | 409 |
| CD302 | CX3CL1 | P78423 | 408 |
| CD302 | HSPB8 | Q9UJY1 | 392 |
| CD302 | SLC27A3 | Q5K4L6 | 384 |
| CD302 | SEC14L2 | O76054 | 379 |
IntAct
33 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| CD302 | IL7R | psi-mi:“MI:0915”(physical association) | 0.560 |
| CD302 | IL10RA | psi-mi:“MI:0915”(physical association) | 0.560 |
| CD302 | FNDC9 | psi-mi:“MI:0915”(physical association) | 0.560 |
| CD302 | ERGIC3 | psi-mi:“MI:0915”(physical association) | 0.560 |
| IL7R | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| IL10RA | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| CD53 | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| OPRM1 | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| IFNGR2 | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| CD302 | GPX8 | psi-mi:“MI:0915”(physical association) | 0.560 |
| GET1 | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| ARL13B | CD302 | psi-mi:“MI:0915”(physical association) | 0.560 |
| METTL3 | TUBAL3 | psi-mi:“MI:0914”(association) | 0.350 |
| FAM171A2 | psi-mi:“MI:0914”(association) | 0.350 | |
| CD302 | ERGIC3 | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | CD53 | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | OPRM1 | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | IFNGR2 | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | GPX8 | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | ARL13B | psi-mi:“MI:0915”(physical association) | 0.000 |
| CD302 | GET1 | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (12): FATE1 (Two-hybrid), CD302 (Affinity Capture-MS), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Two-hybrid), CD302 (Affinity Capture-MS), CD302 (Affinity Capture-MS), CD302 (Affinity Capture-Western)
ESM2 similar proteins: A0A7H0DND3, A1XRN2, A8WH72, A8WH74, A8WH75, A8WUV1, B1A4M7, B1A4N2, B1A4N8, B1A4P2, B1A4P6, B1A4P7, B1A4P8, B1A4P9, B1A4Q0, B1A4Q2, B1A4Q3, B1A4Q5, B1A4Q6, B1A4Q8, B1A4Q9, B1A4R0, B1A4R4, B2D1Y0, O55159, P0DQP8, P10721, P16234, P21057, P21755, P21756, P24761, P24765, P26618, P26619, P33851, Q16YE7, Q1L867, Q3T0L5, Q5FVR3
Diamond homologs: A8WH72, A8WH74, A8WH75, Q02988, Q5FVR3, Q8IX05, Q9DCG2, O45824, P49260, Q60767, Q91ZX1, Q9PSM5
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
10 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 8 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
846 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 2:159777933:CTTA:C | donor_loss | 1.0000 |
| 2:159777934:TTA:T | donor_loss | 1.0000 |
| 2:159777935:TA:T | donor_loss | 1.0000 |
| 2:159777936:A:T | donor_loss | 1.0000 |
| 2:159777937:C:CG | donor_loss | 1.0000 |
| 2:159777961:GGGA:G | acceptor_gain | 1.0000 |
| 2:159777965:C:CC | acceptor_gain | 1.0000 |
| 2:159779999:ACTT:A | donor_loss | 1.0000 |
| 2:159780001:TT:T | donor_loss | 1.0000 |
| 2:159780001:TTA:T | donor_loss | 1.0000 |
| 2:159780002:TA:T | donor_loss | 1.0000 |
| 2:159780003:A:AC | donor_gain | 1.0000 |
| 2:159780003:A:T | donor_loss | 1.0000 |
| 2:159780003:ACTAG:A | donor_gain | 1.0000 |
| 2:159780004:C:CA | donor_loss | 1.0000 |
| 2:159780004:C:CC | donor_gain | 1.0000 |
| 2:159780004:CT:C | donor_gain | 1.0000 |
| 2:159780004:CTA:C | donor_gain | 1.0000 |
| 2:159780004:CTAG:C | donor_gain | 1.0000 |
| 2:159780004:CTAGC:C | donor_gain | 1.0000 |
| 2:159780878:TTA:T | donor_loss | 1.0000 |
| 2:159780879:TA:T | donor_loss | 1.0000 |
| 2:159780880:A:AC | donor_gain | 1.0000 |
| 2:159780880:A:T | donor_loss | 1.0000 |
| 2:159780880:AC:A | donor_gain | 1.0000 |
| 2:159780880:ACCAT:A | donor_gain | 1.0000 |
| 2:159780881:C:CC | donor_gain | 1.0000 |
| 2:159780881:C:CG | donor_loss | 1.0000 |
| 2:159780881:C:CT | donor_loss | 1.0000 |
| 2:159780881:CC:C | donor_gain | 1.0000 |
AlphaMissense
1538 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 2:159780060:C:A | W138C | 0.998 |
| 2:159780060:C:G | W138C | 0.998 |
| 2:159780162:C:A | W104C | 0.997 |
| 2:159780162:C:G | W104C | 0.997 |
| 2:159780062:A:G | W138R | 0.996 |
| 2:159780062:A:T | W138R | 0.996 |
| 2:159780016:C:G | C153S | 0.993 |
| 2:159780017:A:T | C153S | 0.993 |
| 2:159780164:A:G | W104R | 0.993 |
| 2:159780164:A:T | W104R | 0.993 |
| 2:159783370:C:G | C56S | 0.992 |
| 2:159783371:A:T | C56S | 0.992 |
| 2:159783371:A:G | C56R | 0.988 |
| 2:159780129:C:A | W115C | 0.987 |
| 2:159780129:C:G | W115C | 0.987 |
| 2:159780980:A:T | I66K | 0.987 |
| 2:159783369:A:C | C56W | 0.986 |
| 2:159780017:A:G | C153R | 0.985 |
| 2:159780015:G:C | C153W | 0.984 |
| 2:159780016:C:T | C153Y | 0.982 |
| 2:159780061:C:G | W138S | 0.982 |
| 2:159780092:A:G | C128R | 0.982 |
| 2:159780046:C:G | C143S | 0.981 |
| 2:159780047:A:T | C143S | 0.981 |
| 2:159780091:C:G | C128S | 0.979 |
| 2:159780092:A:T | C128S | 0.979 |
| 2:159780980:A:C | I66R | 0.979 |
| 2:159780982:G:C | S65R | 0.979 |
| 2:159780982:G:T | S65R | 0.979 |
| 2:159780984:T:G | S65R | 0.979 |
dbSNP variants (sampled 300 via entrez): RS1000026673 (2:159789003 T>C), RS1000071193 (2:159777069 T>C,G), RS1000242066 (2:159775900 T>G), RS1000250223 (2:159782567 TACAA>T), RS1000352494 (2:159769754 C>T), RS1000403869 (2:159782440 G>A,C,T), RS1000549648 (2:159795222 CG>C,CGG), RS1000561141 (2:159784013 A>G), RS1000579684 (2:159777137 G>A,C), RS1000655401 (2:159787903 G>C), RS1000822467 (2:159771409 A>G), RS1000891579 (2:159769955 T>C,G), RS1000962225 (2:159775736 C>A), RS1001046313 (2:159795686 A>C), RS1001086571 (2:159771038 A>C)
Disease associations
OMIM: gene MIM:612246 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
3 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST007277_3 | Tourette syndrome | 2.000000e-07 |
| GCST009391_1633 | Metabolite levels | 9.000000e-07 |
| GCST012490_496 | Femur bone mineral density x serum urate levels interaction | 2.000000e-08 |
EFO canonical traits (2, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0007787 | plasma betaine measurement |
| EFO:0004531 | urate measurement |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
45 total (human), top 30 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Valproic Acid | affects cotreatment, increases expression, affects expression | 9 |
| bisphenol A | increases expression, affects cotreatment | 2 |
| Dexamethasone | increases expression, affects cotreatment | 2 |
| Cyclosporine | decreases expression | 2 |
| aristolochic acid I | decreases expression | 1 |
| bisphenol F | affects cotreatment, increases expression | 1 |
| quercitrin | decreases expression | 1 |
| terbufos | increases methylation | 1 |
| trichostatin A | increases expression | 1 |
| tris(1,3-dichloro-2-propyl)phosphate | decreases expression | 1 |
| di-n-butylphosphoric acid | affects expression | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| entinostat | increases expression | 1 |
| monomethylarsonous acid | increases expression | 1 |
| 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide | increases expression, affects cotreatment | 1 |
| dorsomorphin | affects cotreatment, increases expression | 1 |
| jinfukang | affects cotreatment, increases expression | 1 |
| NSC 689534 | affects binding, decreases expression | 1 |
| Dasatinib | increases expression | 1 |
| Acetaminophen | decreases expression | 1 |
| Air Pollutants | affects expression, increases abundance | 1 |
| Benzo(a)pyrene | decreases expression | 1 |
| Bilirubin | decreases expression | 1 |
| Cadmium | increases expression | 1 |
| Cisplatin | affects cotreatment, increases expression | 1 |
| Copper | affects binding, decreases expression | 1 |
| Doxorubicin | decreases expression | 1 |
| Fonofos | increases methylation | 1 |
| Ethyl Methanesulfonate | decreases expression | 1 |
| Formaldehyde | 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.