ZNF766

gene
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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

FieldValue
HGNC IDHGNC:28063
Approved symbolZNF766
Namezinc finger protein 766
Location19q13.41
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000196214
Ensembl biotypeprotein_coding
Entrez90321

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

ExonStartEnd
ENSE000014247935229006652296046
ENSE000017428575226958752269631
ENSE000034790065228211152282237
ENSE000036771385228328552283413

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 IDTPM avgSamples expressed
17729610.55571746
1772950.7442469
1772940.2633102
2089170.01414

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
spermCL:000001996.20gold quality
calcaneal tendonUBERON:000370192.09gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047390.61gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.97gold quality
epithelial cell of pancreasCL:000008387.90silver quality
tendonUBERON:000004387.84gold quality
secondary oocyteCL:000065585.75gold quality
colonic epitheliumUBERON:000039785.49gold quality
islet of LangerhansUBERON:000000684.80gold quality
tendon of biceps brachiiUBERON:000818884.75gold quality
amniotic fluidUBERON:000017384.73gold quality
palpebral conjunctivaUBERON:000181284.45gold quality
ganglionic eminenceUBERON:000402384.21gold quality
cortical plateUBERON:000534383.93gold quality
bone marrow cellCL:000209283.69gold quality
upper leg skinUBERON:000426283.58gold quality
testisUBERON:000047383.20gold quality
right testisUBERON:000453483.01gold quality
tibiaUBERON:000097982.85gold quality
cartilage tissueUBERON:000241882.79gold quality
endothelial cellCL:000011582.60silver quality
left testisUBERON:000453382.49gold quality
cardiac muscle of right atriumUBERON:000337982.31silver quality
leukocyteCL:000073882.30gold quality
bone marrowUBERON:000237182.23gold quality
monocyteCL:000057682.12gold quality
adrenal tissueUBERON:001830382.01gold quality
stromal cell of endometriumCL:000225581.77gold quality
parietal pleuraUBERON:000240081.74gold quality
left ventricle myocardiumUBERON:000656681.45silver quality

Single-cell (SCXA)

Detected in 3 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-MTAB-6379no1019.54
E-GEOD-111727no245.48
E-ANND-3no0.00

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2098.1ZNF766More 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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-4789-5P99.9870.762721
HSA-MIR-1236-3P99.9468.041695
HSA-MIR-6845-3P99.9466.881439
HSA-MIR-130599.9171.433443
HSA-MIR-6848-3P99.6466.49885
HSA-MIR-513A-3P99.3970.633620
HSA-MIR-513C-3P99.3970.633620
HSA-MIR-520F-5P99.3470.401632
HSA-MIR-324-3P99.2666.311034
HSA-MIR-6843-3P99.2666.42915
HSA-MIR-6504-3P99.1769.312891
HSA-MIR-10399-5P99.1769.872610
HSA-MIR-3606-3P99.1169.843254
HSA-MIR-29A-5P99.0868.591813
HSA-MIR-939-3P98.9765.072347
HSA-MIR-138-2-3P98.9168.331643
HSA-MIR-6715B-3P98.8068.071204
HSA-MIR-806098.6166.931187
HSA-MIR-147A98.3366.40795
HSA-MIR-6509-3P98.3267.331343
HSA-MIR-6773-3P98.1765.511213
HSA-MIR-197-3P98.0969.231004
HSA-MIR-607298.0066.47804
HSA-MIR-6511B-5P97.9865.64823
HSA-MIR-6811-5P97.9864.96848
HSA-MIR-6810-3P97.9664.571023
HSA-MIR-315997.9466.791098
HSA-MIR-1271-3P97.5664.85865
HSA-MIR-550A-3-5P97.5665.35823

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 766Q5HY98 (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)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_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)

ModelpLDDTFraction very-high
AF-Q5HY98-F166.080.25

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:

CategoryTerms
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
cis-regulatory region sequence-specific DNA binding1
chromatin1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transition metal ion binding1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

506 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF766CCDC97Q96F63400
ZNF766ZSWIM5Q9P217391
ZNF766TRIM28Q13263374
ZNF766MRPL36Q9P0J6357
ZNF766ONECUT3O60422335
ZNF766MRPL42Q9Y6G3325
ZNF766SH3BP4Q9P0V3288
ZNF766ZRANB2O95218265
ZNF766ZBED1O96006265
ZNF766SETDB1Q15047261
ZNF766FOXN2P32314260
ZNF766RNF138Q8WVD3258
ZNF766GEMIN5Q8TEQ6248
ZNF766IL5RAQ01344246
ZNF766RPL28P46779230

IntAct

12 interactions, top by confidence:

ABTypeScore
ZNF766FHL5psi-mi:“MI:0915”(physical association)0.560
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
CPSF7WWP2psi-mi:“MI:0914”(association)0.350
TRIM28ZNF320psi-mi:“MI:0914”(association)0.350
NOTCH2ZNF320psi-mi:“MI:0914”(association)0.350
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
RPL13POLRMTpsi-mi:“MI:0914”(association)0.350
ZNF766FHL5psi-mi:“MI:0915”(physical association)0.000
MDM2ZNF766psi-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):

ClassificationCount (floor)
Pathogenic1
Likely pathogenic0
Uncertain significance52
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (1)

Variant IDHGVSClassification
3779559NM_001010851.3(ZNF766):c.274+2804_274+2806delPathogenic

SpliceAI

618 predictions. Top by Δscore:

VariantEffectΔscore
19:52269628:GCGC:Gdonor_gain1.0000
19:52269630:GC:Gdonor_gain1.0000
19:52269632:G:GGdonor_gain1.0000
19:52282238:G:GAdonor_loss1.0000
19:52282238:G:GGdonor_gain1.0000
19:52282239:T:TCdonor_loss1.0000
19:52269627:GGCGC:Gdonor_gain0.9900
19:52269628:GCGCG:Gdonor_gain0.9900
19:52269629:CGC:Cdonor_gain0.9900
19:52269630:GCG:Gdonor_gain0.9900
19:52269631:CG:Cdonor_loss0.9900
19:52269632:G:GAdonor_loss0.9900
19:52269633:T:Adonor_loss0.9900
19:52269634:G:GCdonor_loss0.9900
19:52282236:GG:Gdonor_gain0.9900
19:52282237:GG:Gdonor_gain0.9900
19:52283362:A:Tdonor_gain0.9900
19:52269635:A:ACdonor_loss0.9800
19:52282109:A:AGacceptor_gain0.9800
19:52282110:G:GGacceptor_gain0.9800
19:52282110:GGGAC:Gacceptor_gain0.9800
19:52282198:G:Tdonor_gain0.9800
19:52269629:C:Tdonor_gain0.9700
19:52269636:G:Cdonor_loss0.9700
19:52282107:TTA:Tacceptor_loss0.9700
19:52282109:AG:Aacceptor_gain0.9700
19:52282109:AGG:Aacceptor_gain0.9700
19:52282109:AGGG:Aacceptor_loss0.9700
19:52282110:GG:Gacceptor_gain0.9700
19:52282110:GGG:Gacceptor_gain0.9700

AlphaMissense

3125 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:52291049:T:CF420L0.991
19:52291051:C:AF420L0.991
19:52291051:C:GF420L0.991
19:52290965:T:CF392L0.990
19:52290967:C:AF392L0.990
19:52290967:C:GF392L0.990
19:52290881:T:CF364L0.987
19:52290883:T:AF364L0.987
19:52290883:T:GF364L0.987
19:52290990:G:CR400P0.981
19:52291056:A:CQ422P0.980
19:52290994:T:AH401Q0.979
19:52290994:T:GH401Q0.979
19:52290996:A:CQ402P0.978
19:52291006:C:AH405Q0.976
19:52291006:C:GH405Q0.976
19:52290992:C:GH401D0.974
19:52291078:T:AH429Q0.974
19:52291078:T:GH429Q0.974
19:52291080:A:CQ430P0.974
19:52282144:T:CF18L0.972
19:52282146:C:AF18L0.972
19:52282146:C:GF18L0.972
19:52290797:T:CF336L0.972
19:52290799:T:AF336L0.972
19:52290799:T:GF336L0.972
19:52291050:T:CF420S0.971
19:52290966:T:CF392S0.969
19:52290629:T:CF280L0.967
19:52290631:C:AF280L0.967

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):

StudyTraitp-value
GCST002916_14Cannabis use (initiation)4.000000e-06

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0007586Cannabis 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.

ChemicalActions (top 5)PubMed papers
Phenylmercuric Acetateaffects cotreatment, decreases expression2
Cyclosporineincreases expression2
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
beta-lapachoneincreases expression1
sodium arsenitedecreases expression1
di-n-butylphosphoric acidaffects expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamidedecreases expression, affects cotreatment1
dorsomorphinaffects cotreatment, decreases expression1
MT19c compoundincreases expression1
Air Pollutantsaffects expression, increases abundance1
Atrazineincreases expression1
Cadmiumincreases abundance, increases expression1
Doxorubicindecreases expression1
Ethyl Methanesulfonateincreases expression1
Formaldehydedecreases expression1
Methyl Methanesulfonateincreases expression1
Ozoneaffects expression, increases abundance1
Phthalic Acidsdecreases methylation1
Potassium Chloridedecreases expression, decreases response to substance1
Dronabinoldecreases response to substance, decreases expression1
Valproic Aciddecreases expression1
Cadmium Chlorideincreases abundance, increases expression1

Cellosaurus cell lines

1 cell lines: 1 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_HA09K562 eGFP-ZNF766Cancer cell lineFemale

Clinical trials (associated diseases)

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

  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): hypercalcemia, infantile, 1