ZNF766
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Summary
ZNF766 (zinc finger protein 766, HGNC:28063) is a protein-coding gene on chromosome 19q13.41, encoding Zinc finger protein 766 (Q5HY98). May be involved in transcriptional regulation.
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus.
Source: NCBI Gene 90321 — RefSeq curated summary.
At a glance
- GWAS associations: 1
- Clinical variants (ClinVar): 62 total — 1 pathogenic
- MANE Select transcript:
NM_001010851
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:28063 |
| Approved symbol | ZNF766 |
| Name | zinc finger protein 766 |
| Location | 19q13.41 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000196214 |
| Ensembl biotype | protein_coding |
| Entrez | 90321 |
Gene structure
Transcript identifiers
Ensembl transcripts: 10 — 9 protein_coding, 1 retained_intron
ENST00000439461, ENST00000593612, ENST00000593703, ENST00000595000, ENST00000595149, ENST00000599581, ENST00000600016, ENST00000600821, ENST00000601711, ENST00000950441
RefSeq mRNA: 1 — MANE Select: NM_001010851
NM_001010851
CCDS: CCDS46163
Canonical transcript exons
ENST00000439461 — 4 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001424793 | 52290066 | 52296046 |
| ENSE00001742857 | 52269587 | 52269631 |
| ENSE00003479006 | 52282111 | 52282237 |
| ENSE00003677138 | 52283285 | 52283413 |
Expression profiles
Bgee: expression breadth ubiquitous, 251 present calls, max score 96.20.
FANTOM5 (CAGE): breadth ubiquitous, TPM avg 11.5773 / max 230.9802, expressed in 1759 samples.
FANTOM5 promoters (4 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 177296 | 10.5557 | 1746 |
| 177295 | 0.7442 | 469 |
| 177294 | 0.2633 | 102 |
| 208917 | 0.0141 | 4 |
Top tissues by expression
256 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| sperm | CL:0000019 | 96.20 | gold quality |
| calcaneal tendon | UBERON:0003701 | 92.09 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 90.61 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 87.97 | gold quality |
| epithelial cell of pancreas | CL:0000083 | 87.90 | silver quality |
| tendon | UBERON:0000043 | 87.84 | gold quality |
| secondary oocyte | CL:0000655 | 85.75 | gold quality |
| colonic epithelium | UBERON:0000397 | 85.49 | gold quality |
| islet of Langerhans | UBERON:0000006 | 84.80 | gold quality |
| tendon of biceps brachii | UBERON:0008188 | 84.75 | gold quality |
| amniotic fluid | UBERON:0000173 | 84.73 | gold quality |
| palpebral conjunctiva | UBERON:0001812 | 84.45 | gold quality |
| ganglionic eminence | UBERON:0004023 | 84.21 | gold quality |
| cortical plate | UBERON:0005343 | 83.93 | gold quality |
| bone marrow cell | CL:0002092 | 83.69 | gold quality |
| upper leg skin | UBERON:0004262 | 83.58 | gold quality |
| testis | UBERON:0000473 | 83.20 | gold quality |
| right testis | UBERON:0004534 | 83.01 | gold quality |
| tibia | UBERON:0000979 | 82.85 | gold quality |
| cartilage tissue | UBERON:0002418 | 82.79 | gold quality |
| endothelial cell | CL:0000115 | 82.60 | silver quality |
| left testis | UBERON:0004533 | 82.49 | gold quality |
| cardiac muscle of right atrium | UBERON:0003379 | 82.31 | silver quality |
| leukocyte | CL:0000738 | 82.30 | gold quality |
| bone marrow | UBERON:0002371 | 82.23 | gold quality |
| monocyte | CL:0000576 | 82.12 | gold quality |
| adrenal tissue | UBERON:0018303 | 82.01 | gold quality |
| stromal cell of endometrium | CL:0002255 | 81.77 | gold quality |
| parietal pleura | UBERON:0002400 | 81.74 | gold quality |
| left ventricle myocardium | UBERON:0006566 | 81.45 | silver quality |
Single-cell (SCXA)
Detected in 3 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-6379 | no | 1019.54 |
| E-GEOD-111727 | no | 245.48 |
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: yes
JASPAR motifs
| Motif | Name | Family |
|---|---|---|
| MA2098.1 | ZNF766 | More than 3 adjacent zinc fingers |
JASPAR matrix evidence (PMIDs): PMID:22955616
miRNA regulators (miRDB)
40 targeting ZNF766, 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-548C-3P | 99.99 | 74.01 | 7587 |
| HSA-MIR-4789-5P | 99.98 | 70.76 | 2721 |
| HSA-MIR-1236-3P | 99.94 | 68.04 | 1695 |
| HSA-MIR-6845-3P | 99.94 | 66.88 | 1439 |
| HSA-MIR-1305 | 99.91 | 71.43 | 3443 |
| HSA-MIR-6848-3P | 99.64 | 66.49 | 885 |
| HSA-MIR-513A-3P | 99.39 | 70.63 | 3620 |
| HSA-MIR-513C-3P | 99.39 | 70.63 | 3620 |
| HSA-MIR-520F-5P | 99.34 | 70.40 | 1632 |
| HSA-MIR-324-3P | 99.26 | 66.31 | 1034 |
| HSA-MIR-6843-3P | 99.26 | 66.42 | 915 |
| HSA-MIR-6504-3P | 99.17 | 69.31 | 2891 |
| HSA-MIR-10399-5P | 99.17 | 69.87 | 2610 |
| HSA-MIR-3606-3P | 99.11 | 69.84 | 3254 |
| HSA-MIR-29A-5P | 99.08 | 68.59 | 1813 |
| HSA-MIR-939-3P | 98.97 | 65.07 | 2347 |
| HSA-MIR-138-2-3P | 98.91 | 68.33 | 1643 |
| HSA-MIR-6715B-3P | 98.80 | 68.07 | 1204 |
| HSA-MIR-8060 | 98.61 | 66.93 | 1187 |
| HSA-MIR-147A | 98.33 | 66.40 | 795 |
| HSA-MIR-6509-3P | 98.32 | 67.33 | 1343 |
| HSA-MIR-6773-3P | 98.17 | 65.51 | 1213 |
| HSA-MIR-197-3P | 98.09 | 69.23 | 1004 |
| HSA-MIR-6072 | 98.00 | 66.47 | 804 |
| HSA-MIR-6511B-5P | 97.98 | 65.64 | 823 |
| HSA-MIR-6811-5P | 97.98 | 64.96 | 848 |
| HSA-MIR-6810-3P | 97.96 | 64.57 | 1023 |
| HSA-MIR-3159 | 97.94 | 66.79 | 1098 |
| HSA-MIR-1271-3P | 97.56 | 64.85 | 865 |
| HSA-MIR-550A-3-5P | 97.56 | 65.35 | 823 |
Cross-species orthologs
0 orthologs
Paralogs (11): ZNF761 (ENSG00000160336), ZNF701 (ENSG00000167562), ZNF816 (ENSG00000180257), ZNF765 (ENSG00000196417), ZNF860 (ENSG00000197385), ZNF813 (ENSG00000198346), ZNF525 (ENSG00000203326), ZNF468 (ENSG00000204604), ZNF888 (ENSG00000213793), ZNF578 (ENSG00000258405), (ENSG00000269825)
Protein
Protein identifiers
Zinc finger protein 766 — Q5HY98 (reviewed: Q5HY98)
All UniProt accessions (8): A0A0B4J2B2, G3XAE0, M0QXI4, M0R139, M0R1P9, M0R2P3, M0R2R1, Q5HY98
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 (1): NP_001010851* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR001909 | KRAB | Domain |
| IPR013087 | Znf_C2H2_type | Domain |
| IPR036051 | KRAB_dom_sf | Homologous_superfamily |
| IPR036236 | Znf_C2H2_sf | Homologous_superfamily |
Pfam: PF00096, PF01352, PF13465
UniProt features (18 total): zinc finger region 10, cross-link 4, chain 1, domain 1, sequence variant 1, sequence conflict 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q5HY98-F1 | 66.08 | 0.25 |
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 (4): 75, 157, 179, 367
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 40 (showing top):
GOCC_MICROTUBULE_ORGANIZING_CENTER, GOCC_CENTROSOME, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, FIGUEROA_AML_METHYLATION_CLUSTER_1_UP, FIGUEROA_AML_METHYLATION_CLUSTER_4_UP, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, CBX5_TARGET_GENES, HES2_TARGET_GENES, ZNF350_TARGET_GENES, MIR1236_3P, MIR1227_3P, GSE13485_CTRL_VS_DAY21_YF17D_VACCINE_PBMC_UP, SAFB2_TARGET_GENES, POU2AF1_TARGET_GENES, DESCARTES_MAIN_FETAL_CORNEAL_AND_CONJUNCTIVAL_EPITHELIAL_CELLS
GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)
GO Molecular Function (6): RNA polymerase II cis-regulatory region sequence-specific DNA binding (GO:0000978), DNA-binding transcription factor activity, RNA polymerase II-specific (GO:0000981), zinc ion binding (GO:0008270), DNA binding (GO:0003677), protein binding (GO:0005515), 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 |
|---|---|
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 2 |
| regulation of DNA-templated transcription | 1 |
| transcription by RNA polymerase II | 1 |
| DNA-templated transcription | 1 |
| regulation of gene expression | 1 |
| regulation of RNA biosynthetic process | 1 |
| cis-regulatory region sequence-specific DNA binding | 1 |
| chromatin | 1 |
| DNA-binding transcription factor activity | 1 |
| regulation of transcription by RNA polymerase II | 1 |
| transition metal ion binding | 1 |
| nucleic acid binding | 1 |
| binding | 1 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
506 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF766 | CCDC97 | Q96F63 | 400 |
| ZNF766 | ZSWIM5 | Q9P217 | 391 |
| ZNF766 | TRIM28 | Q13263 | 374 |
| ZNF766 | MRPL36 | Q9P0J6 | 357 |
| ZNF766 | ONECUT3 | O60422 | 335 |
| ZNF766 | MRPL42 | Q9Y6G3 | 325 |
| ZNF766 | SH3BP4 | Q9P0V3 | 288 |
| ZNF766 | ZRANB2 | O95218 | 265 |
| ZNF766 | ZBED1 | O96006 | 265 |
| ZNF766 | SETDB1 | Q15047 | 261 |
| ZNF766 | FOXN2 | P32314 | 260 |
| ZNF766 | RNF138 | Q8WVD3 | 258 |
| ZNF766 | GEMIN5 | Q8TEQ6 | 248 |
| ZNF766 | IL5RA | Q01344 | 246 |
| ZNF766 | RPL28 | P46779 | 230 |
IntAct
12 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| ZNF766 | FHL5 | psi-mi:“MI:0915”(physical association) | 0.560 |
| TRIM28 | ZNF320 | psi-mi:“MI:0914”(association) | 0.530 |
| CPSF7 | WWP2 | psi-mi:“MI:0914”(association) | 0.350 |
| TRIM28 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| NOTCH2 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| LTBP2 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| RPL13 | POLRMT | psi-mi:“MI:0914”(association) | 0.350 |
| ZNF766 | FHL5 | psi-mi:“MI:0915”(physical association) | 0.000 |
| MDM2 | ZNF766 | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (12): ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Two-hybrid), ZNF766 (Affinity Capture-RNA), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-MS), ZNF766 (Affinity Capture-RNA)
ESM2 similar proteins: A0A1W2PQL4, A0JPL0, A2RRD8, A6NHJ4, A6NP11, B4DX44, O75346, O95780, P0CB33, P21506, P51508, P52738, Q0D2J5, Q0VGE8, Q12901, Q13360, Q14593, Q15973, Q2M218, Q2M3X9, Q2VY69, Q3SXZ3, Q5HY98, Q5RCJ2, Q5VIY5, Q6J6I6, Q7L2R6, Q86XU0, Q86Y25, Q8IW36, Q8IYN0, Q8IYX0, Q8N782, Q8N883, Q8N9Z0, Q8NDP4, Q95K49, Q969W8, Q96H40, Q96N58
Diamond homologs: A0A1W2PQL4, A6NK75, A6NN14, A6NNF4, A6NP11, A8MQ14, A8MTY0, A8MUV8, A8MXY4, B4DX44, B4DXR9, E9PYI1, O14628, O43345, O75290, O75346, O75373, O75437, O95780, P0CB33, P0DKX0, P0DPD5, P16373, P17019, P17038, P21506, P35789, P52736, P52738, P52744, Q03923, Q03924, Q03936, Q03938, Q05481, Q14586, Q14593, Q14929, Q15928, Q3KNS6
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
62 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 1 |
| Likely pathogenic | 0 |
| Uncertain significance | 52 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (1)
| Variant ID | HGVS | Classification |
|---|---|---|
| 3779559 | NM_001010851.3(ZNF766):c.274+2804_274+2806del | Pathogenic |
SpliceAI
618 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:52269628:GCGC:G | donor_gain | 1.0000 |
| 19:52269630:GC:G | donor_gain | 1.0000 |
| 19:52269632:G:GG | donor_gain | 1.0000 |
| 19:52282238:G:GA | donor_loss | 1.0000 |
| 19:52282238:G:GG | donor_gain | 1.0000 |
| 19:52282239:T:TC | donor_loss | 1.0000 |
| 19:52269627:GGCGC:G | donor_gain | 0.9900 |
| 19:52269628:GCGCG:G | donor_gain | 0.9900 |
| 19:52269629:CGC:C | donor_gain | 0.9900 |
| 19:52269630:GCG:G | donor_gain | 0.9900 |
| 19:52269631:CG:C | donor_loss | 0.9900 |
| 19:52269632:G:GA | donor_loss | 0.9900 |
| 19:52269633:T:A | donor_loss | 0.9900 |
| 19:52269634:G:GC | donor_loss | 0.9900 |
| 19:52282236:GG:G | donor_gain | 0.9900 |
| 19:52282237:GG:G | donor_gain | 0.9900 |
| 19:52283362:A:T | donor_gain | 0.9900 |
| 19:52269635:A:AC | donor_loss | 0.9800 |
| 19:52282109:A:AG | acceptor_gain | 0.9800 |
| 19:52282110:G:GG | acceptor_gain | 0.9800 |
| 19:52282110:GGGAC:G | acceptor_gain | 0.9800 |
| 19:52282198:G:T | donor_gain | 0.9800 |
| 19:52269629:C:T | donor_gain | 0.9700 |
| 19:52269636:G:C | donor_loss | 0.9700 |
| 19:52282107:TTA:T | acceptor_loss | 0.9700 |
| 19:52282109:AG:A | acceptor_gain | 0.9700 |
| 19:52282109:AGG:A | acceptor_gain | 0.9700 |
| 19:52282109:AGGG:A | acceptor_loss | 0.9700 |
| 19:52282110:GG:G | acceptor_gain | 0.9700 |
| 19:52282110:GGG:G | acceptor_gain | 0.9700 |
AlphaMissense
3125 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:52291049:T:C | F420L | 0.991 |
| 19:52291051:C:A | F420L | 0.991 |
| 19:52291051:C:G | F420L | 0.991 |
| 19:52290965:T:C | F392L | 0.990 |
| 19:52290967:C:A | F392L | 0.990 |
| 19:52290967:C:G | F392L | 0.990 |
| 19:52290881:T:C | F364L | 0.987 |
| 19:52290883:T:A | F364L | 0.987 |
| 19:52290883:T:G | F364L | 0.987 |
| 19:52290990:G:C | R400P | 0.981 |
| 19:52291056:A:C | Q422P | 0.980 |
| 19:52290994:T:A | H401Q | 0.979 |
| 19:52290994:T:G | H401Q | 0.979 |
| 19:52290996:A:C | Q402P | 0.978 |
| 19:52291006:C:A | H405Q | 0.976 |
| 19:52291006:C:G | H405Q | 0.976 |
| 19:52290992:C:G | H401D | 0.974 |
| 19:52291078:T:A | H429Q | 0.974 |
| 19:52291078:T:G | H429Q | 0.974 |
| 19:52291080:A:C | Q430P | 0.974 |
| 19:52282144:T:C | F18L | 0.972 |
| 19:52282146:C:A | F18L | 0.972 |
| 19:52282146:C:G | F18L | 0.972 |
| 19:52290797:T:C | F336L | 0.972 |
| 19:52290799:T:A | F336L | 0.972 |
| 19:52290799:T:G | F336L | 0.972 |
| 19:52291050:T:C | F420S | 0.971 |
| 19:52290966:T:C | F392S | 0.969 |
| 19:52290629:T:C | F280L | 0.967 |
| 19:52290631:C:A | F280L | 0.967 |
dbSNP variants (sampled 300 via entrez): RS1000000713 (19:52278160 A>G), RS1000102521 (19:52289399 A>C,G,T), RS1000245302 (19:52273278 G>T), RS1000456929 (19:52268079 A>G), RS1000653812 (19:52274976 C>A), RS1000660289 (19:52275294 CAAG>C), RS1000783893 (19:52269483 G>A), RS1000912388 (19:52294196 G>A,C), RS1000928570 (19:52292848 T>C), RS1000979133 (19:52269746 C>T), RS1001237471 (19:52268596 T>A,C), RS1001253671 (19:52295356 G>T), RS1001290991 (19:52283549 T>A), RS1001445723 (19:52273371 T>C), RS1001484731 (19:52278812 C>T)
Disease associations
OMIM: gene `` | disease phenotypes: MIM:143880
GenCC curated gene-disease
Mondo (1): hypercalcemia, infantile, 1 (MONDO:0020739)
Orphanet (1): Autosomal recessive infantile hypercalcemia (Orphanet:300547)
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
1 associations (top):
| Study | Trait | p-value |
|---|---|---|
| GCST002916_14 | Cannabis use (initiation) | 4.000000e-06 |
EFO canonical traits (1, from GWAS)
| EFO ID | Trait name |
|---|---|
| EFO:0007586 | Cannabis use initiation |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
24 total (human), top 24 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Phenylmercuric Acetate | affects cotreatment, decreases expression | 2 |
| Cyclosporine | increases expression | 2 |
| 3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamide | decreases expression | 1 |
| TAK-243 | increases sumoylation | 1 |
| triphenyl phosphate | affects expression | 1 |
| beta-lapachone | increases expression | 1 |
| sodium arsenite | decreases expression | 1 |
| di-n-butylphosphoric acid | affects expression | 1 |
| 4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamide | decreases expression, affects cotreatment | 1 |
| dorsomorphin | affects cotreatment, decreases expression | 1 |
| MT19c compound | increases expression | 1 |
| Air Pollutants | affects expression, increases abundance | 1 |
| Atrazine | increases expression | 1 |
| Cadmium | increases abundance, increases expression | 1 |
| Doxorubicin | decreases expression | 1 |
| Ethyl Methanesulfonate | increases expression | 1 |
| Formaldehyde | decreases expression | 1 |
| Methyl Methanesulfonate | increases expression | 1 |
| Ozone | affects expression, increases abundance | 1 |
| Phthalic Acids | decreases methylation | 1 |
| Potassium Chloride | decreases expression, decreases response to substance | 1 |
| Dronabinol | decreases response to substance, decreases expression | 1 |
| Valproic Acid | decreases expression | 1 |
| Cadmium Chloride | increases abundance, increases expression | 1 |
Cellosaurus cell lines
1 cell lines: 1 cancer cell line
First 10 cell lines (id-ordered, not curated):
| Cellosaurus | Name | Category | Sex |
|---|---|---|---|
| CVCL_HA09 | K562 eGFP-ZNF766 | Cancer cell line | Female |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): hypercalcemia, infantile, 1