ZNF566

gene
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Also known as FLJ14779MGC12515

Summary

ZNF566 (zinc finger protein 566, HGNC:25919) is a protein-coding gene on chromosome 19q13.12, encoding Zinc finger protein 566 (Q969W8). May be involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus.

Source: NCBI Gene 84924 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 21 total
  • MANE Select transcript: NM_001145344

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25919
Approved symbolZNF566
Namezinc finger protein 566
Location19q13.12
Locus typegene with protein product
StatusApproved
AliasesFLJ14779, MGC12515
Ensembl geneENSG00000186017
Ensembl biotypeprotein_coding
Entrez84924

Gene structure

Transcript identifiers

Ensembl transcripts: 16 — 12 protein_coding, 3 retained_intron, 1 protein_coding_CDS_not_defined

ENST00000392170, ENST00000424129, ENST00000427002, ENST00000434377, ENST00000452939, ENST00000460937, ENST00000472909, ENST00000480361, ENST00000493391, ENST00000494354, ENST00000587567, ENST00000915907, ENST00000915908, ENST00000915909, ENST00000915910, ENST00000968795

RefSeq mRNA: 5 — MANE Select: NM_001145344 NM_001145343, NM_001145344, NM_001145345, NM_001300970, NM_032838

CCDS: CCDS12494, CCDS46061, CCDS74346

Canonical transcript exons

ENST00000452939 — 5 exons

ExonStartEnd
ENSE000011150203647291136473006
ENSE000016008003648948636489561
ENSE000017961773644511936450001
ENSE000024943513647333236473458
ENSE000036686583647654936476616

Expression profiles

Bgee: expression breadth ubiquitous, 192 present calls, max score 86.76.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 5.0556 / max 66.4794, expressed in 1557 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
1806762.37341139
1806771.3790790
1806790.9774549
1806780.3257148

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.76gold quality
cortical plateUBERON:000534384.12gold quality
calcaneal tendonUBERON:000370183.33gold quality
ganglionic eminenceUBERON:000402383.19gold quality
ventricular zoneUBERON:000305381.21gold quality
hindlimb stylopod muscleUBERON:000425279.20gold quality
adrenal tissueUBERON:001830379.04gold quality
colonic epitheliumUBERON:000039777.84gold quality
islet of LangerhansUBERON:000000677.80gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.72gold quality
cerebellar hemisphereUBERON:000224577.51gold quality
cerebellar cortexUBERON:000212977.37gold quality
cerebellumUBERON:000203776.19gold quality
stromal cell of endometriumCL:000225575.89gold quality
right hemisphere of cerebellumUBERON:001489075.74gold quality
muscle of legUBERON:000138375.44gold quality
smooth muscle tissueUBERON:000113575.35gold quality
gastrocnemiusUBERON:000138875.10gold quality
C1 segment of cervical spinal cordUBERON:000646975.04gold quality
Brodmann (1909) area 9UBERON:001354074.62gold quality
mucosa of stomachUBERON:000119974.56gold quality
left uterine tubeUBERON:000130374.34gold quality
left adrenal glandUBERON:000123474.11gold quality
granulocyteCL:000009473.99gold quality
left adrenal gland cortexUBERON:003582573.81gold quality
anterior cingulate cortexUBERON:000983573.61gold quality
descending thoracic aortaUBERON:000234573.57gold quality
lower esophagus muscularis layerUBERON:003583373.56gold quality
lower esophagusUBERON:001347373.55gold quality
prefrontal cortexUBERON:000045173.40gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-GEOD-124858no136.36
E-ANND-3no4.53

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

176 targeting ZNF566, 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-1277-5P100.0073.955056
HSA-MIR-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-5692A100.0074.406850
HSA-MIR-200B-3P100.0073.312693
HSA-MIR-200C-3P100.0073.352685
HSA-MIR-429100.0073.442698
HSA-MIR-340-5P100.0072.504437
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-3163100.0077.238605
HSA-MIR-30A-5P100.0076.313233
HSA-MIR-30B-5P100.0076.293248
HSA-MIR-30C-5P100.0076.293248
HSA-MIR-30D-5P100.0076.323233
HSA-MIR-30E-5P100.0076.323242
HSA-MIR-520G-5P99.9966.76658
HSA-MIR-450099.9972.722367
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-318599.9968.121959
HSA-MIR-366299.9973.825684
HSA-MIR-477599.9875.006394
HSA-LET-7A-5P99.9872.291790
HSA-LET-7B-5P99.9872.311790
HSA-LET-7C-5P99.9872.291790
HSA-LET-7E-5P99.9872.291790
HSA-LET-7F-5P99.9872.561784
HSA-LET-7G-5P99.9872.371784
HSA-LET-7I-5P99.9872.371788
HSA-MIR-98-5P99.9872.331787
HSA-MIR-373-5P99.9875.364753

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
mus_musculusZfp566ENSMUSG00000078768
rattus_norvegicusZfp566ENSRNOG00000048138
drosophila_melanogasterCG2712FBGN0024975
drosophila_melanogasterPhsFBGN0036522
drosophila_melanogasterCG3281FBGN0260741

Paralogs (62): ZNF582 (ENSG00000018869), ZNF264 (ENSG00000083844), ZNF343 (ENSG00000088876), ZNF684 (ENSG00000117010), ZNF133 (ENSG00000125846), ZNF557 (ENSG00000130544), ZNF337 (ENSG00000130684), ZNF20 (ENSG00000132010), ZFP37 (ENSG00000136866), ZNF614 (ENSG00000142556), KRBOX4 (ENSG00000147121), ZNF599 (ENSG00000153896), ZNF19 (ENSG00000157429), ZNF589 (ENSG00000164048), PRDM9 (ENSG00000164256), ZNF180 (ENSG00000167384), ZNF558 (ENSG00000167785), ZNF35 (ENSG00000169981), ZNF778 (ENSG00000170100), ZNF439 (ENSG00000171291), ZNF440 (ENSG00000171295), ZNF556 (ENSG00000172000), ZNF554 (ENSG00000172006), ZNF596 (ENSG00000172748), ZNF80 (ENSG00000174255), ZNF266 (ENSG00000174652), ZNF25 (ENSG00000175395), ZNF77 (ENSG00000175691), ZNF169 (ENSG00000175787), ZNF404 (ENSG00000176222), ZNF491 (ENSG00000177599), ZNF620 (ENSG00000177842), ZNF619 (ENSG00000177873), ZNF875 (ENSG00000181666), ZNF329 (ENSG00000181894), ZFP90 (ENSG00000184939), ZNF529 (ENSG00000186020), ZNF749 (ENSG00000186230), ZNF555 (ENSG00000186300), ZNF70 (ENSG00000187792)

Protein

Protein identifiers

Zinc finger protein 566Q969W8 (reviewed: Q969W8)

All UniProt accessions (5): Q969W8, B4DRR6, C9J2D3, C9J6X1, K7EQC1

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.

Isoforms (2)

UniProt IDNamesCanonical?
Q969W8-11yes
Q969W8-22

RefSeq proteins (5): NP_001138815, NP_001138816, NP_001138817, NP_001287899, NP_116227 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050758Znf_C2H2-typeFamily

Pfam: PF00096, PF01352, PF13465

UniProt features (13 total): zinc finger region 8, cross-link 2, chain 1, domain 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q969W8-F168.050.21

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 (2): 314, 328

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 115 (showing top): MODULE_255, GCM_ZNF198, MODULE_317, GCM_PPM1D, GCM_SUFU, WEBER_METHYLATED_IN_COLON_CANCER, MODULE_69, KRIGE_RESPONSE_TO_TOSEDOSTAT_24HR_UP, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MODULE_37, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, BANP_TARGET_GENES, IRF5_TARGET_GENES, NFE2L1_TARGET_GENES, SUPT16H_TARGET_GENES

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 transcription regulatory region sequence-specific DNA binding (GO:0000977), 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 (2): nucleus (GO:0005634), membrane (GO:0016020)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
RNA Polymerase II Transcription1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transcription cis-regulatory region binding1
chromatin1
RNA polymerase II transcription regulatory region sequence-specific DNA binding1
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
cellular anatomical structure1

Protein interactions and networks

STRING

508 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF566PDZK1IP1Q13113477
ZNF566MBD3L3A6NE82431
ZNF566ZNF608Q9ULD9375
ZNF566C8orf89P0DMQ9375
ZNF566ZFHX3Q15911370
ZNF566SP140LQ9H930322
ZNF566ZNF804AQ7Z570311
ZNF566PITX2Q99697310
ZNF566GMEB1Q9Y692305
ZNF566ENTPD6O75354290
ZNF566INO80EQ8NBZ0290
ZNF566FAM133AQ8N9E0276
ZNF566CMC2Q9NRP2266
ZNF566ETV7Q9Y603256
ZNF566SACK1BQ5T0W9248

IntAct

23 interactions, top by confidence:

ABTypeScore
EXOC8ZNF566psi-mi:“MI:0915”(physical association)0.560
MAGOHBZNF566psi-mi:“MI:0915”(physical association)0.560
ZNF566MAGOHBpsi-mi:“MI:0915”(physical association)0.560
ZNF566KIF9psi-mi:“MI:0915”(physical association)0.560
ZNF566SPRED1psi-mi:“MI:0915”(physical association)0.560
TRIM28ZNF316psi-mi:“MI:0914”(association)0.530
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
Trim28FTH1psi-mi:“MI:0915”(physical association)0.400
ZNF566KIF2Cpsi-mi:“MI:0915”(physical association)0.370
SPATA20SCRN3psi-mi:“MI:0914”(association)0.350
CBX5ZNF568psi-mi:“MI:0914”(association)0.350
ZNF566IPO8psi-mi:“MI:0914”(association)0.350
SPATA20HDAC4psi-mi:“MI:0914”(association)0.350
TRIM63ZNF566psi-mi:“MI:0915”(physical association)0.000
TRIM55ZNF566psi-mi:“MI:0915”(physical association)0.000
KIF9ZNF566psi-mi:“MI:0915”(physical association)0.000

BioGRID (23): ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Synthetic Lethality), ZNF566 (Two-hybrid), ZNF566 (Two-hybrid), ZNF566 (Two-hybrid), ZNF566 (Two-hybrid), ZNF566 (Two-hybrid), ZNF566 (Proximity Label-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS), ZNF566 (Affinity Capture-MS)

ESM2 similar proteins: A0A087WUV0, A0JNB1, A2VDP4, B2RUI1, P0CG31, P10072, P17025, P17036, P17097, P18733, P51814, Q08ER8, Q09FC8, Q0VGE8, Q14590, Q15937, Q16600, Q2M3X9, Q4V8A8, Q5CZA5, Q5R8G9, Q5RBX0, Q5VIY5, Q68DI1, Q6J6I6, Q6NX49, Q6P1L6, Q6PG37, Q6ZMS4, Q6ZMW2, Q80YP6, Q86UD4, Q86Y25, Q8IZ26, Q8N184, Q8NB42, Q8NEK5, Q8TAF7, Q8TF47, Q8WXB4

Diamond homologs: A0A1W2PQL4, A0JNB1, A0JPL0, A6NK53, A6QLU5, A6QPT6, A7MBI1, A8MT65, A8MUV8, A8MWA4, B2RXC5, B4DU55, B4DX44, E9PYI1, O14628, O75346, P0CH99, P0CI00, P17014, P17030, P17032, P17098, P51786, P85977, Q02386, Q06730, Q06732, Q0VAW7, Q12901, Q13360, Q14586, Q14588, Q14590, Q16587, Q2M3X9, Q2VY69, Q32M78, Q3ZCX4, Q49AA0, Q4R6J4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

21 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance9
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1079 predictions. Top by Δscore:

VariantEffectΔscore
19:36450002:C:CCacceptor_gain1.0000
19:36473326:CCTTA:Cdonor_loss1.0000
19:36473327:CTT:Cdonor_loss1.0000
19:36473328:TTA:Tdonor_loss1.0000
19:36473329:TA:Tdonor_loss1.0000
19:36473330:A:ATdonor_loss1.0000
19:36473330:AC:Adonor_gain1.0000
19:36473331:CC:Cdonor_gain1.0000
19:36449997:CAGGA:Cacceptor_gain0.9900
19:36449998:AGGA:Aacceptor_gain0.9900
19:36449999:GGA:Gacceptor_gain0.9900
19:36449999:GGAC:Gacceptor_loss0.9900
19:36450000:GA:Gacceptor_gain0.9900
19:36450000:GAC:Gacceptor_loss0.9900
19:36450001:AC:Aacceptor_loss0.9900
19:36473011:T:Cacceptor_gain0.9900
19:36473330:A:ACdonor_gain0.9900
19:36473331:C:CCdonor_gain0.9900
19:36473456:CTC:Cacceptor_gain0.9900
19:36473458:CCTGG:Cacceptor_loss0.9900
19:36473460:T:Cacceptor_loss0.9900
19:36476612:TAGAG:Tacceptor_gain0.9900
19:36476617:C:CCacceptor_gain0.9900
19:36481737:A:Tacceptor_gain0.9900
19:36450003:T:Cacceptor_loss0.9800
19:36473011:T:TCacceptor_gain0.9800
19:36473459:C:CCacceptor_gain0.9800
19:36476542:ATCT:Adonor_loss0.9800
19:36476543:TCTCA:Tdonor_loss0.9800
19:36476544:CTCAC:Cdonor_loss0.9800

AlphaMissense

1558 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:36473377:A:CY31D0.981
19:36473400:A:GL23P0.979
19:36473408:C:AW20C0.977
19:36473408:C:GW20C0.977
19:36449610:A:CF208L0.976
19:36449610:A:TF208L0.976
19:36449612:A:GF208L0.976
19:36473410:A:GW20R0.974
19:36473410:A:TW20R0.974
19:36473424:A:GF15S0.969
19:36473343:A:GL42P0.967
19:36449585:G:CH217D0.963
19:36449583:A:CH217Q0.955
19:36449583:A:TH217Q0.955
19:36473376:T:GY31S0.952
19:36449553:A:CF227L0.949
19:36449553:A:TF227L0.949
19:36449555:A:GF227L0.949
19:36473423:G:CF15L0.947
19:36473423:G:TF15L0.947
19:36473425:A:GF15L0.947
19:36473409:C:GW20S0.943
19:36449581:T:GQ218P0.942
19:36473444:G:CF8L0.940
19:36473444:G:TF8L0.940
19:36473446:A:GF8L0.940
19:36449539:C:GC232S0.938
19:36449540:A:TC232S0.938
19:36473377:A:TY31N0.938
19:36449538:A:CC232W0.937

dbSNP variants (sampled 300 via entrez): RS1000054786 (19:36469656 G>A), RS1000104729 (19:36459499 C>T), RS1000282859 (19:36453117 CA>C,CAA,CAAA), RS1000461785 (19:36449706 A>G), RS1000612846 (19:36477778 T>C), RS1000663525 (19:36482148 C>A), RS1000666625 (19:36477468 A>T), RS1000690060 (19:36465053 C>T), RS1000777970 (19:36482306 C>T), RS1000781060 (19:36478957 G>A), RS1000873400 (19:36483984 T>C,G), RS1000940792 (19:36467924 G>A), RS1001043749 (19:36446534 C>G), RS1001060139 (19:36468097 A>G), RS1001069610 (19:36489766 C>A,G,T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

20 total (human), top 20 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, decreases expression3
aristolochic acid Idecreases expression1
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
coumarinincreases phosphorylation1
di-n-butylphosphoric acidaffects expression1
Vorinostatdecreases expression1
Air Pollutantsdecreases expression, increases abundance1
Air Pollutants, Occupationaldecreases expression1
Benzo(a)pyreneincreases methylation1
Nickeldecreases expression1
Oxygendecreases expression1
Testosteroneincreases expression1
Tetrachlorodibenzodioxindecreases expression1
Tretinoindecreases expression1
Cyclosporinedecreases expression1
Aflatoxin B1increases methylation1
Cadmium Chloridedecreases expression1
Particulate Matterincreases abundance, decreases expression1

Clinical trials (associated diseases)

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

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.