ZNF787
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Summary
ZNF787 (zinc finger protein 787, HGNC:26998) is a protein-coding gene on chromosome 19q13.43, encoding Zinc finger protein 787 (Q6DD87). May be involved in transcriptional regulation.
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.
Source: NCBI Gene 126208 — RefSeq curated summary.
At a glance
- GWAS associations: 4
- Clinical variants (ClinVar): 56 total
- Druggable target: yes
- MANE Select transcript:
NM_001002836
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:26998 |
| Approved symbol | ZNF787 |
| Name | zinc finger protein 787 |
| Location | 19q13.43 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000142409 |
| Ensembl biotype | protein_coding |
| Entrez | 126208 |
Gene structure
Transcript identifiers
Ensembl transcripts: 10 — 10 protein_coding
ENST00000586787, ENST00000587279, ENST00000610935, ENST00000969467, ENST00000969468, ENST00000969469, ENST00000969470, ENST00000969471, ENST00000969472, ENST00000969473
RefSeq mRNA: 2 — MANE Select: NM_001002836
NM_001002836, NM_001351682
CCDS: CCDS42634, CCDS86810
Canonical transcript exons
ENST00000610935 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003711520 | 56103139 | 56103227 |
| ENSE00003711686 | 56121172 | 56121295 |
| ENSE00003740286 | 56087366 | 56089092 |
Expression profiles
Bgee: expression breadth ubiquitous, 237 present calls, max score 91.59.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 25.5028 / max 490.8687, expressed in 1816 samples.
FANTOM5 promoters (2 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 182864 | 23.9840 | 1815 |
| 182865 | 1.5189 | 876 |
Top tissues by expression
284 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| hindlimb stylopod muscle | UBERON:0004252 | 91.59 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 91.50 | gold quality |
| right uterine tube | UBERON:0001302 | 90.86 | gold quality |
| apex of heart | UBERON:0002098 | 90.54 | gold quality |
| gastrocnemius | UBERON:0001388 | 90.21 | gold quality |
| right lobe of liver | UBERON:0001114 | 89.56 | gold quality |
| muscle of leg | UBERON:0001383 | 89.03 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 88.84 | gold quality |
| granulocyte | CL:0000094 | 88.62 | gold quality |
| monocyte | CL:0000576 | 88.33 | gold quality |
| mononuclear cell | CL:0000842 | 87.98 | gold quality |
| leukocyte | CL:0000738 | 87.82 | gold quality |
| transverse colon | UBERON:0001157 | 87.26 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 87.11 | gold quality |
| body of stomach | UBERON:0001161 | 87.00 | gold quality |
| body of pancreas | UBERON:0001150 | 86.75 | gold quality |
| muscle layer of sigmoid colon | UBERON:0035805 | 86.13 | gold quality |
| lower esophagus muscularis layer | UBERON:0035833 | 86.05 | gold quality |
| lower esophagus | UBERON:0013473 | 86.04 | gold quality |
| blood | UBERON:0000178 | 85.91 | gold quality |
| left adrenal gland cortex | UBERON:0035825 | 85.86 | gold quality |
| left adrenal gland | UBERON:0001234 | 85.83 | gold quality |
| heart left ventricle | UBERON:0002084 | 85.73 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 85.51 | gold quality |
| cardiac ventricle | UBERON:0002082 | 85.14 | gold quality |
| left uterine tube | UBERON:0001303 | 85.10 | gold quality |
| spleen | UBERON:0002106 | 84.93 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 84.85 | gold quality |
| right atrium auricular region | UBERON:0006631 | 84.81 | gold quality |
| right adrenal gland | UBERON:0001233 | 84.80 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | yes | 4.72 |
| E-MTAB-6075 | no | 28.76 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
19 targeting ZNF787, 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-371A-3P | 99.99 | 66.77 | 91 |
| HSA-MIR-4656 | 98.79 | 66.22 | 1306 |
| HSA-MIR-330-5P | 98.73 | 67.63 | 1788 |
| HSA-MIR-3180 | 98.46 | 64.68 | 348 |
| HSA-MIR-3180-3P | 98.46 | 64.68 | 348 |
| HSA-MIR-6816-5P | 98.46 | 64.35 | 364 |
| HSA-MIR-1910-3P | 98.44 | 67.51 | 1695 |
| HSA-MIR-326 | 98.25 | 66.44 | 1565 |
| HSA-MIR-6511A-5P | 98.13 | 67.47 | 1770 |
| HSA-MIR-33B-3P | 97.92 | 67.39 | 529 |
| HSA-MIR-515-3P | 97.92 | 67.98 | 506 |
| HSA-MIR-519E-3P | 97.92 | 68.25 | 508 |
| HSA-MIR-3920 | 97.75 | 69.02 | 1168 |
| HSA-MIR-6787-5P | 97.54 | 63.85 | 457 |
| HSA-MIR-10396B-5P | 94.99 | 63.57 | 358 |
| HSA-MIR-1908-5P | 94.99 | 63.41 | 352 |
| HSA-MIR-663A | 94.99 | 63.54 | 378 |
| HSA-MIR-371B-3P | 94.48 | 66.59 | 345 |
| HSA-MIR-25-5P | 87.02 | 64.95 | 84 |
Literature-anchored findings (GeneRIF, showing 1)
- ZNF787 and HDAC1 Mediate Blood-Brain Barrier Permeability in an In Vitro Model of Alzheimer’s Disease Microenvironment. (PMID:38329647)
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Zfp787 | ENSMUSG00000046792 |
| rattus_norvegicus | Zfp787 | ENSRNOG00000015456 |
Paralogs (1): ZNF316 (ENSG00000205903)
Protein
Protein identifiers
Zinc finger protein 787 — Q6DD87 (reviewed: Q6DD87)
Alternative names: TTF-I-interacting peptide 20
All UniProt accessions (3): Q6DD87, K7EKJ5, M0R0X7
UniProt curated annotations — full annotation on UniProt →
Function. May be involved in transcriptional regulation.
Subcellular location. Nucleus.
Similarity. Belongs to the krueppel C2H2-type zinc-finger protein family.
RefSeq proteins (2): NP_001002836, NP_001338611 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR013087 | Znf_C2H2_type | Domain |
| IPR036236 | Znf_C2H2_sf | Homologous_superfamily |
| IPR050527 |
Pfam: PF00096, PF13465, PF13912
UniProt features (19 total): zinc finger region 7, modified residue 3, cross-link 2, sequence conflict 2, region of interest 2, chain 1, compositionally biased region 1, sequence variant 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q6DD87-F1 | 65.10 | 0.00 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Post-translational modifications (5): 117, 122, 132, 191, 211
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 53 (showing top):
YAGI_AML_WITH_INV_16_TRANSLOCATION, DARWICHE_SKIN_TUMOR_PROMOTER_DN, DARWICHE_PAPILLOMA_RISK_LOW_DN, DARWICHE_PAPILLOMA_RISK_HIGH_DN, DARWICHE_SQUAMOUS_CELL_CARCINOMA_DN, DARWICHE_PAPILLOMA_PROGRESSION_RISK, RASHI_RESPONSE_TO_IONIZING_RADIATION_5, GRADE_COLON_AND_RECTAL_CANCER_DN, IVANOVA_HEMATOPOIESIS_EARLY_PROGENITOR, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, CYCLIN_D1_KE_.V1_UP, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ELF2_TARGET_GENES, SNIP1_TARGET_GENES, UBN1_TARGET_GENES
GO Biological Process (1): regulation of transcription by RNA polymerase II (GO:0006357)
GO Molecular Function (6): DNA-binding transcription factor activity, RNA polymerase II-specific (GO:0000981), zinc ion binding (GO:0008270), sequence-specific DNA binding (GO:0043565), sequence-specific double-stranded DNA binding (GO:1990837), DNA binding (GO:0003677), metal ion binding (GO:0046872)
GO Cellular Component (1): nucleus (GO:0005634)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| regulation of DNA-templated transcription | 1 |
| transcription by RNA polymerase II | 1 |
| chromatin | 1 |
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 1 |
| DNA-binding transcription factor activity | 1 |
| regulation of transcription by RNA polymerase II | 1 |
| transition metal ion binding | 1 |
| DNA binding | 1 |
| double-stranded DNA binding | 1 |
| sequence-specific DNA binding | 1 |
| nucleic acid binding | 1 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
888 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF787 | BNIP1 | Q12981 | 953 |
| ZNF787 | ZW10 | O43264 | 945 |
| ZNF787 | RINT1 | Q6NUQ1 | 819 |
| ZNF787 | STX18 | Q9P2W9 | 789 |
| ZNF787 | COG4 | Q9H9E3 | 725 |
| ZNF787 | VPS53 | Q5VIR6 | 702 |
| ZNF787 | USE1 | Q9NZ43 | 687 |
| ZNF787 | COG3 | Q96JB2 | 664 |
| ZNF787 | EXOC3 | O60645 | 592 |
| ZNF787 | ANKDD1B | A6NHY2 | 519 |
| ZNF787 | EXOC7 | Q9UPT5 | 512 |
| ZNF787 | VPS54 | Q9P1Q0 | 507 |
| ZNF787 | COG2 | Q14746 | 507 |
| ZNF787 | COG1 | Q8WTW3 | 506 |
| ZNF787 | VPS51 | Q9UID3 | 481 |
IntAct
32 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| CDK5RAP3 | UFL1 | psi-mi:“MI:0914”(association) | 0.870 |
| MOB1B | LATS1 | psi-mi:“MI:0914”(association) | 0.840 |
| STBD1 | GABARAP | psi-mi:“MI:0914”(association) | 0.760 |
| SMARCE1 | SMARCA2 | psi-mi:“MI:0914”(association) | 0.730 |
| P4HA3 | FAM171A2 | psi-mi:“MI:0914”(association) | 0.640 |
| RPL10A | RRP8 | psi-mi:“MI:0914”(association) | 0.640 |
| PNLIP | LAMC1 | psi-mi:“MI:0914”(association) | 0.530 |
| MAGEB2 | GTPBP10 | psi-mi:“MI:0914”(association) | 0.530 |
| ESR1 | ESYT2 | psi-mi:“MI:0914”(association) | 0.350 |
| ORF4a | MPHOSPH10 | psi-mi:“MI:0914”(association) | 0.350 |
| SOX2 | CBX4 | psi-mi:“MI:0914”(association) | 0.350 |
| NOTCH2 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| TMEM63C | GPR89A | psi-mi:“MI:0914”(association) | 0.350 |
| ESYT2 | psi-mi:“MI:0914”(association) | 0.350 | |
| PES1 | psi-mi:“MI:0914”(association) | 0.350 | |
| POLR3A | psi-mi:“MI:0914”(association) | 0.350 | |
| POLRMT | psi-mi:“MI:0914”(association) | 0.350 | |
| SUPT5H | psi-mi:“MI:0914”(association) | 0.350 | |
| GTPBP10 | psi-mi:“MI:0914”(association) | 0.350 | |
| DDX3X | psi-mi:“MI:0914”(association) | 0.350 | |
| FGFBP1 | psi-mi:“MI:0914”(association) | 0.350 | |
| ZNF460 | TOMM40 | psi-mi:“MI:0914”(association) | 0.350 |
| H1-1 | POLRMT | psi-mi:“MI:0914”(association) | 0.350 |
| SLC11A1 | TRAFD1 | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (55): ZNF787 (Affinity Capture-RNA), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-RNA), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Proximity Label-MS), ZNF787 (Proximity Label-MS), ZNF787 (Proximity Label-MS), ZNF787 (Proximity Label-MS), ZNF787 (Affinity Capture-MS), ZNF787 (Affinity Capture-MS)
ESM2 similar proteins: A2CE44, A6NFI3, A6NM28, A8K8V0, O15370, O70218, O95201, P0CJ78, P10075, P10754, P28698, P70338, Q04890, Q07120, Q14V87, Q19A40, Q569E7, Q58DK7, Q5DWN0, Q5FWU5, Q5RJR4, Q5T619, Q5TEC3, Q6DD87, Q6IQX8, Q6PD29, Q6PGE4, Q6ZMY9, Q7Z7K2, Q80VM4, Q8BIF9, Q8JZL0, Q8N8E2, Q8NAF0, Q8NCA9, Q8TD94, Q8WUU4, Q96C55, Q96H86, Q96MX3
Diamond homologs: A1L2U9, A2A884, A2ANX9, A7Y7X5, B0X9H6, B0YDH7, B1WAZ8, B1WBU4, E9PW05, E9PZZ1, G5EBU4, O15391, O60315, O62836, O75362, O77459, O95863, P08048, P0CS62, P0CS63, P10925, P15822, P17010, P17012, P20662, P22227, P25490, P28166, P31509, P31629, P36197, P52739, P52746, P56270, P56670, P56671, P60319, P80944, Q00899, Q00900
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
56 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 49 |
| Likely benign | 5 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
1190 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:56089088:GTCCA:G | acceptor_gain | 1.0000 |
| 19:56089089:TCCA:T | acceptor_gain | 1.0000 |
| 19:56089090:CCA:C | acceptor_gain | 1.0000 |
| 19:56089090:CCAC:C | acceptor_gain | 1.0000 |
| 19:56089091:CA:C | acceptor_gain | 1.0000 |
| 19:56089091:CAC:C | acceptor_gain | 1.0000 |
| 19:56089091:CACTG:C | acceptor_loss | 1.0000 |
| 19:56089092:ACTG:A | acceptor_loss | 1.0000 |
| 19:56089093:C:CC | acceptor_gain | 1.0000 |
| 19:56089094:T:A | acceptor_loss | 1.0000 |
| 19:56103133:GCTCA:G | donor_loss | 1.0000 |
| 19:56103134:CTCA:C | donor_loss | 1.0000 |
| 19:56103135:TCA:T | donor_loss | 1.0000 |
| 19:56103136:CA:C | donor_loss | 1.0000 |
| 19:56103137:ACCTG:A | donor_loss | 1.0000 |
| 19:56103226:CC:C | acceptor_gain | 1.0000 |
| 19:56103227:CC:C | acceptor_gain | 1.0000 |
| 19:56103228:C:CC | acceptor_gain | 1.0000 |
| 19:56103231:T:C | acceptor_gain | 1.0000 |
| 19:56103231:T:TC | acceptor_gain | 1.0000 |
| 19:56121173:T:TA | donor_gain | 1.0000 |
| 19:56089101:C:CT | acceptor_gain | 0.9900 |
| 19:56089102:A:T | acceptor_gain | 0.9900 |
| 19:56103223:GGTCC:G | acceptor_gain | 0.9900 |
| 19:56103224:GTCC:G | acceptor_gain | 0.9900 |
| 19:56103225:TCC:T | acceptor_gain | 0.9900 |
| 19:56103226:CCC:C | acceptor_gain | 0.9900 |
| 19:56103228:C:T | acceptor_gain | 0.9900 |
| 19:56103230:G:C | acceptor_gain | 0.9900 |
| 19:56103241:A:C | acceptor_gain | 0.9900 |
AlphaMissense
2483 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:56088611:G:C | F187L | 1.000 |
| 19:56088611:G:T | F187L | 1.000 |
| 19:56088613:A:G | F187L | 1.000 |
| 19:56088695:G:C | F159L | 1.000 |
| 19:56088695:G:T | F159L | 1.000 |
| 19:56088697:A:G | F159L | 1.000 |
| 19:56088779:G:C | F131L | 1.000 |
| 19:56088779:G:T | F131L | 1.000 |
| 19:56088781:A:G | F131L | 1.000 |
| 19:56088863:G:C | F103L | 1.000 |
| 19:56088863:G:T | F103L | 1.000 |
| 19:56088865:A:G | F103L | 1.000 |
| 19:56088908:G:C | H88Q | 1.000 |
| 19:56088908:G:T | H88Q | 1.000 |
| 19:56088947:A:C | F75L | 1.000 |
| 19:56088947:A:T | F75L | 1.000 |
| 19:56088949:A:G | F75L | 1.000 |
| 19:56088194:G:C | F326L | 0.999 |
| 19:56088194:G:T | F326L | 0.999 |
| 19:56088196:A:G | F326L | 0.999 |
| 19:56088612:A:G | F187S | 0.999 |
| 19:56088634:A:G | C180R | 0.999 |
| 19:56088696:A:G | F159S | 0.999 |
| 19:56088707:G:C | C155W | 0.999 |
| 19:56088718:A:G | C152R | 0.999 |
| 19:56088740:G:C | H144Q | 0.999 |
| 19:56088740:G:T | H144Q | 0.999 |
| 19:56088742:G:C | H144D | 0.999 |
| 19:56088747:C:G | R142P | 0.999 |
| 19:56088750:T:G | Q141P | 0.999 |
dbSNP variants (sampled 300 via entrez): RS1000075019 (19:56087734 C>G,T), RS1000214491 (19:56112197 A>G), RS1000228939 (19:56116063 T>C), RS1000293411 (19:56122175 A>G), RS1000302446 (19:56089558 G>A), RS1000402355 (19:56090085 G>A), RS1000407915 (19:56103319 G>A,T), RS1000447711 (19:56116898 T>G), RS1000537634 (19:56102713 T>C,G), RS1000621886 (19:56098012 G>A,T), RS1000622612 (19:56112585 T>C), RS1000662205 (19:56098760 T>TG), RS1000714751 (19:56107607 G>A), RS1000768406 (19:56102322 C>G,T), RS1000831436 (19:56093458 C>G,T)
Disease associations
OMIM: gene `` | disease phenotypes: MIM:157900
GenCC curated gene-disease
Mondo (1): Mobius syndrome (MONDO:0008006)
Orphanet (1): Moebius syndrome (Orphanet:570)
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
4 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST005194_209 | Coronary artery disease | 4.000000e-06 |
| GCST005991_73 | Platelet count | 2.000000e-17 |
| GCST012282_10 | BMI x environmental factors (excluding physical activity) interaction | 3.000000e-06 |
| GCST012283_6 | BMI x environmental factors (including physical activity) interaction | 2.000000e-06 |
EFO canonical traits (9, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0004309 | platelet count |
| EFO:0004340 | body mass index |
| EFO:0006527 | smoking status measurement |
| EFO:0009374 | energy intake measurement |
| EFO:0009695 | household income |
| EFO:0010810 | protein intake measurement |
| EFO:0010811 | carbohydrate intake measurement |
| EFO:0011015 | educational attainment |
| EFO:0008002 | physical activity measurement |
MeSH disease descriptors (1)
| Descriptor | Name | Tree numbers |
|---|---|---|
| D020331 | Mobius Syndrome | C07.465.299.825; C10.292.319.825; C10.292.562.700.375.750; C11.590.436.400.750; C16.131.077.578; C16.614.595 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: yes
ChEMBL targets (1): CHEMBL6067428 (SINGLE PROTEIN)
PharmGKB: 1 entry (VIP=true, CPIC=false)
ChEMBL bioactivities
2 potent at pChembl≥5 of 2 total, top 2 by pChembl (potency: 10 = 0.1 nM, 6 = 1 µM).
| pChembl | Type | Value | Unit | Molecule |
|---|---|---|---|---|
| 7.50 | Kd | 31.75 | nM | CHEMBL5653589 |
| 7.50 | ED50 | 31.75 | nM | CHEMBL5653589 |
PubChem BioAssay actives
1 with measured affinity, of 2 total; 1 most potent distinct compounds. Largely complementary to BindingDB; screening values are coarse (µM, 4 dp), so sub-nM hits tie at the floor.
| Compound | Assay | Type | Value | Unit |
|---|---|---|---|---|
| 4-methyl-3-[(2-methyl-6-pyridin-3-ylpyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-[3-(trifluoromethyl)phenyl]benzamide | 2149817: Binding affinity to human ZNF787 incubated for 45 mins by Kinobead based pull down assay | kd | 0.0318 | uM |
CTD chemical–gene interactions
36 total (human), top 30 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| bisphenol F | increases expression, affects cotreatment | 2 |
| sodium arsenite | decreases expression, increases expression | 2 |
| Air Pollutants | increases abundance, increases expression, affects expression | 2 |
| Tobacco Smoke Pollution | increases expression, increases methylation | 2 |
| Valproic Acid | decreases expression, increases methylation | 2 |
| FR900359 | affects phosphorylation | 1 |
| TAK-243 | increases sumoylation | 1 |
| triphenyl phosphate | affects expression | 1 |
| propylparaben | increases expression | 1 |
| lead acetate | increases expression | 1 |
| trichostatin A | affects expression | 1 |
| zinc chromate | increases abundance, decreases expression | 1 |
| benzo(e)pyrene | decreases methylation | 1 |
| cupric chloride | increases expression | 1 |
| chromium hexavalent ion | decreases expression, increases abundance | 1 |
| nutlin 3 | affects cotreatment, increases secretion | 1 |
| ICG 001 | increases expression | 1 |
| abrine | increases expression | 1 |
| 2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide | decreases expression, affects cotreatment | 1 |
| (+)-JQ1 compound | decreases expression | 1 |
| Bortezomib | increases expression | 1 |
| Arsenic | affects methylation | 1 |
| Benzo(a)pyrene | affects methylation, increases methylation | 1 |
| Cisplatin | decreases expression | 1 |
| Dactinomycin | affects cotreatment, increases secretion | 1 |
| Dexamethasone | affects cotreatment, increases expression | 1 |
| Doxorubicin | decreases expression | 1 |
| Indomethacin | increases expression, affects cotreatment | 1 |
| Ivermectin | decreases expression | 1 |
| Methapyrilene | decreases methylation | 1 |
ChEMBL screening assays
1 unique, capped per target: 1 binding
Representative assays (with source publication via chembl_document):
| Assay ID | Type | Description | Source paper |
|---|---|---|---|
| CHEMBL5652859 | Binding | Binding affinity to human ZNF787 incubated for 45 mins by Kinobead based pull down assay | NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family. — ChemMedChem |
Clinical trials (associated diseases)
1 trials via MONDO — disease-level, not drug-specific.
| Trial | Phase | Status | Title |
|---|---|---|---|
| NCT03059420 | Not specified | RECRUITING | Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies |
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): Mobius syndrome