ZNF569

gene
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Also known as FLJ32053ZAP1Zfp74

Summary

ZNF569 (zinc finger protein 569, HGNC:24737) is a protein-coding gene on chromosome 19q13.12, encoding Zinc finger protein 569 (Q5MCW4). 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. Predicted to be active in nucleus.

Source: NCBI Gene 148266 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 75 total
  • MANE Select transcript: NM_152484

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:24737
Approved symbolZNF569
Namezinc finger protein 569
Location19q13.12
Locus typegene with protein product
StatusApproved
AliasesFLJ32053, ZAP1, Zfp74
Ensembl geneENSG00000196437
Ensembl biotypeprotein_coding
OMIM613904
Entrez148266

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 18 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000316950, ENST00000392149, ENST00000392150, ENST00000448051, ENST00000589833, ENST00000591073, ENST00000591710, ENST00000592490, ENST00000882774, ENST00000882775, ENST00000882776, ENST00000882777, ENST00000882778, ENST00000882779, ENST00000940356, ENST00000940357, ENST00000943077, ENST00000943078, ENST00000943079

RefSeq mRNA: 2 — MANE Select: NM_152484 NM_001330482, NM_152484

CCDS: CCDS12503, CCDS82341

Canonical transcript exons

ENST00000316950 — 6 exons

ExonStartEnd
ENSE000013645753746531337465473
ENSE000013731733746708437467444
ENSE000024851173742586837425963
ENSE000034859293744490737444964
ENSE000037910353742625237426378
ENSE000038907253741115737414419

Expression profiles

Bgee: expression breadth ubiquitous, 218 present calls, max score 87.83.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 8.2702 / max 84.4849, expressed in 1556 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
1807143.58251331
1807162.2337941
1807152.1340986
1807130.191280
1807120.128641

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099187.83gold quality
spermCL:000001986.08gold quality
oocyteCL:000002385.89gold quality
cortical plateUBERON:000534385.30gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047383.81gold quality
ganglionic eminenceUBERON:000402383.68gold quality
secondary oocyteCL:000065581.69gold quality
ventricular zoneUBERON:000305381.25gold quality
calcaneal tendonUBERON:000370180.08gold quality
right testisUBERON:000453479.43gold quality
left testisUBERON:000453379.33gold quality
testisUBERON:000047378.90gold quality
sural nerveUBERON:001548877.84gold quality
islet of LangerhansUBERON:000000677.13gold quality
cerebellar cortexUBERON:000212974.57gold quality
cerebellar hemisphereUBERON:000224574.45gold quality
prefrontal cortexUBERON:000045174.29gold quality
adrenal tissueUBERON:001830374.29gold quality
hindlimb stylopod muscleUBERON:000425274.26gold quality
smooth muscle tissueUBERON:000113574.09gold quality
cerebellumUBERON:000203773.89gold quality
stromal cell of endometriumCL:000225573.57gold quality
pigmented layer of retinaUBERON:000178273.29gold quality
right hemisphere of cerebellumUBERON:001489073.24gold quality
hypothalamusUBERON:000189872.81gold quality
muscle of legUBERON:000138372.69gold quality
Brodmann (1909) area 9UBERON:001354072.66gold quality
gastrocnemiusUBERON:000138872.54gold quality
anterior cingulate cortexUBERON:000983572.34gold quality
mucosa of paranasal sinusUBERON:000503072.31silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-CURD-10no181.60
E-ANND-3no3.56

Regulation

Is transcription factor: yes

Downstream targets (CollecTRI)

2 targets.

TargetRegulation
ETNK1
SLU7

miRNA regulators (miRDB)

86 targeting ZNF569, 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-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-656-3P100.0072.152788
HSA-MIR-188-3P100.0068.761240
HSA-MIR-190A-3P100.0080.355520
HSA-MIR-428299.9975.366408
HSA-MIR-3692-3P99.9870.272139
HSA-MIR-56899.9869.862084
HSA-MIR-477599.9875.006394
HSA-MIR-807599.9767.20962
HSA-MIR-128-3P99.9571.172484
HSA-MIR-216A-3P99.9571.192505
HSA-MIR-335-3P99.9373.364958
HSA-MIR-311999.9271.342390
HSA-MIR-153-5P99.8973.866317
HSA-MIR-3681-3P99.8870.462254
HSA-MIR-806299.8868.43995
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-576-5P99.8470.462582
HSA-MIR-548AZ-3P99.8270.563549
HSA-MIR-548BC99.8270.613524
HSA-MIR-548E-3P99.8270.593514
HSA-MIR-548F-3P99.8270.593540
HSA-MIR-374C-5P99.8072.062910
HSA-MIR-655-3P99.8072.192909
HSA-MIR-548A-3P99.7670.583524

Literature-anchored findings (GeneRIF, showing 1)

  • ZNF569 protein may act as a transcriptional repressor that suppresses MAPK signaling pathway to mediate cellular functions (PMID:16793018)

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriozgc:66472ENSDARG00000075916
danio_reriosi:ch211-148l7.4ENSDARG00000094469
mus_musculusZfp74ENSMUSG00000059975
rattus_norvegicusZfp74ENSRNOG00000069539
drosophila_melanogastermldFBGN0263490

Paralogs (36): ZNF302 (ENSG00000089335), ZNF184 (ENSG00000096654), CTCF (ENSG00000102974), ZNF574 (ENSG00000105732), ZBTB24 (ENSG00000112365), ZNF142 (ENSG00000115568), CTCFL (ENSG00000124092), ZNF473 (ENSG00000142528), ZNF827 (ENSG00000151612), ZNF689 (ENSG00000156853), ZNF208 (ENSG00000160321), ZNF91 (ENSG00000167232), ZNF526 (ENSG00000167625), ZNF764 (ENSG00000169951), ZNF747 (ENSG00000169955), ZNF282 (ENSG00000170265), ZNF160 (ENSG00000170949), ZNF497 (ENSG00000174586), ZBTB34 (ENSG00000177125), ZNF771 (ENSG00000179965), ZNF48 (ENSG00000180035), ZNF594 (ENSG00000180626), ZBTB37 (ENSG00000185278), ZFP92 (ENSG00000189420), ZNF107 (ENSG00000196247), ZNF729 (ENSG00000196350), ZNF420 (ENSG00000197050), ZNF785 (ENSG00000197162), ZNF665 (ENSG00000197497), ZNF181 (ENSG00000197841), ZNF347 (ENSG00000197937), ZNF84 (ENSG00000198040), ZBTB48 (ENSG00000204859), ZNF845 (ENSG00000213799), ZNF99 (ENSG00000213973), ZNF688 (ENSG00000229809)

Protein

Protein identifiers

Zinc finger protein 569Q5MCW4 (reviewed: Q5MCW4)

All UniProt accessions (5): Q5MCW4, K7EJ12, K7EKE0, K7ELU1, K7ENQ2

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?
Q5MCW4-11yes
Q5MCW4-22

RefSeq proteins (2): NP_001317411, NP_689697* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (24 total): zinc finger region 18, sequence variant 2, chain 1, domain 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5MCW4-F175.490.21

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 112 (showing top): AGCTCCT_MIR28, STAT1_02, KRIGE_RESPONSE_TO_TOSEDOSTAT_24HR_UP, NIKOLSKY_MUTATED_AND_AMPLIFIED_IN_BREAST_CANCER, YKACATTT_UNKNOWN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, STAT1_03, SNACANNNYSYAGA_UNKNOWN, ALX4_01, GSE5503_MLN_DC_VS_SPLEEN_DC_ACTIVATED_ALLOGENIC_TCELL_UP, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ALKBH3_TARGET_GENES, ARID5B_TARGET_GENES, CBX5_TARGET_GENES, CBX7_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 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)

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
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

2048 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF569TRIM28Q13263981
ZNF569ZUP1Q96AP4855
ZNF569USP5P45974818
ZNF569UBBP02248810
ZNF569YOD1Q5VVQ6786
ZNF569USP44Q9H0E7772
ZNF569OTUD7AQ8TE49739
ZNF569SETDB1Q15047673
ZNF569ZPR1O75312670
ZNF569CRBNQ96SW2659
ZNF569HDAC6Q9UBN7653
ZNF569UBA2Q9UBT2648
ZNF569PHF20Q9BVI0638
ZNF569NPLOC4Q8TAT6567
ZNF569ZFAND5O76080552

IntAct

17 interactions, top by confidence:

ABTypeScore
ZNF569KRT31psi-mi:“MI:0915”(physical association)0.720
KRT31ZNF569psi-mi:“MI:0915”(physical association)0.720
KRT40ZNF569psi-mi:“MI:0915”(physical association)0.560
ZNF569KRT40psi-mi:“MI:0915”(physical association)0.560
THZNF569psi-mi:“MI:0915”(physical association)0.560
ZNF569CDC37psi-mi:“MI:0915”(physical association)0.400
CBX5ZNF568psi-mi:“MI:0914”(association)0.350
STK24PIK3C2Apsi-mi:“MI:0914”(association)0.350
STK38LSH3PXD2Bpsi-mi:“MI:2364”(proximity)0.270
ZNF569KRT31psi-mi:“MI:0915”(physical association)0.000
THZNF569psi-mi:“MI:0915”(physical association)0.000

BioGRID (13): ZNF569 (Two-hybrid), ZNF569 (Two-hybrid), ZNF569 (Reconstituted Complex), ZNF569 (Two-hybrid), ZNF569 (Two-hybrid), ZNF569 (Two-hybrid), ZNF569 (Affinity Capture-RNA), ZNF569 (Affinity Capture-MS), ZNF569 (Affinity Capture-MS), ZNF569 (Affinity Capture-MS), ZNF569 (Affinity Capture-MS), ZNF569 (Affinity Capture-RNA), ZNF569 (Affinity Capture-MS)

ESM2 similar proteins: A2VDQ7, A6NNF4, A8MQ14, A8MTY0, E9QAG8, O75290, O75373, P08043, P0CJ79, P10751, P17017, P17027, P17039, P35789, P51522, P51523, Q08AN1, Q14585, Q14587, Q3SYV7, Q3ZCX4, Q4R4C7, Q52M93, Q5MCW4, Q5R5U3, Q5R8X1, Q5R9F0, Q5SXM1, Q6ECI4, Q6JLC9, Q6P3V2, Q6P5C7, Q6ZN57, Q86UE3, Q86XN6, Q86YE8, Q8C827, Q8IYB9, Q8N4W9, Q8N7M2

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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance68
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1183 predictions. Top by Δscore:

VariantEffectΔscore
19:37425960:TAGC:Tacceptor_gain1.0000
19:37425964:C:CCacceptor_gain1.0000
19:37426251:CCTA:Cdonor_gain1.0000
19:37426254:A:ACdonor_gain1.0000
19:37426255:C:CCdonor_gain1.0000
19:37469277:GAC:Gdonor_gain1.0000
19:37425863:CTAA:Cdonor_loss0.9900
19:37425865:AAC:Adonor_loss0.9900
19:37425867:C:Adonor_loss0.9900
19:37425891:T:TAdonor_gain0.9900
19:37425894:T:TAdonor_gain0.9900
19:37425960:TAGCC:Tacceptor_loss0.9900
19:37425961:AGCC:Aacceptor_loss0.9900
19:37425962:GC:Gacceptor_gain0.9900
19:37425963:CC:Cacceptor_gain0.9900
19:37425963:CCTG:Cacceptor_loss0.9900
19:37425965:T:Cacceptor_loss0.9900
19:37426246:TCTTA:Tdonor_loss0.9900
19:37426247:CTTA:Cdonor_loss0.9900
19:37426248:TTA:Tdonor_loss0.9900
19:37426249:TA:Tdonor_loss0.9900
19:37426250:A:Cdonor_loss0.9900
19:37426251:CCTAC:Cdonor_loss0.9900
19:37426377:CC:Cacceptor_gain0.9900
19:37426378:CC:Cacceptor_gain0.9900
19:37426379:C:CCacceptor_gain0.9900
19:37426427:T:TCacceptor_gain0.9900
19:37444902:TTTA:Tdonor_loss0.9900
19:37444903:TTA:Tdonor_loss0.9900
19:37444904:T:TGdonor_loss0.9900

AlphaMissense

4645 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:37412729:G:CF643L0.998
19:37412729:G:TF643L0.998
19:37412731:A:GF643L0.998
19:37412897:G:CF587L0.998
19:37412897:G:TF587L0.998
19:37412899:A:GF587L0.998
19:37412981:G:CF559L0.998
19:37412981:G:TF559L0.998
19:37412983:A:GF559L0.998
19:37413233:A:CF475L0.998
19:37413233:A:TF475L0.998
19:37413235:A:GF475L0.998
19:37412645:G:CF671L0.997
19:37412645:G:TF671L0.997
19:37412647:A:GF671L0.997
19:37412813:G:CF615L0.997
19:37412813:G:TF615L0.997
19:37412815:A:GF615L0.997
19:37413065:G:CF531L0.997
19:37413065:G:TF531L0.997
19:37413067:A:GF531L0.997
19:37413216:A:GL481P0.997
19:37413401:G:CF419L0.997
19:37413401:G:TF419L0.997
19:37413403:A:GF419L0.997
19:37413569:G:CF363L0.997
19:37413569:G:TF363L0.997
19:37413571:A:GF363L0.997
19:37413737:G:CF307L0.997
19:37413737:G:TF307L0.997

dbSNP variants (sampled 300 via entrez): RS1000095520 (19:37463600 A>G), RS1000137171 (19:37456837 A>C,G), RS1000159930 (19:37417364 G>A,C,T), RS1000342424 (19:37437605 C>T), RS1000375132 (19:37437373 T>G), RS1000543001 (19:37430871 T>C), RS1000623143 (19:37444468 C>G), RS1000729222 (19:37410948 C>T), RS1000756132 (19:37418483 A>G), RS1000801628 (19:37465500 A>G), RS1000802066 (19:37445058 A>G), RS1000849434 (19:37418283 C>A,G,T), RS1000883589 (19:37430139 G>A), RS1000911410 (19:37451324 C>A,G,T), RS1000951963 (19:37457192 C>A)

Disease associations

OMIM: gene MIM:613904 | 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

30 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Aciddecreases expression, decreases methylation5
trichostatin Aaffects cotreatment, decreases expression2
sodium arsenitedecreases expression, increases expression2
methacrylaldehydeaffects cotreatment, decreases expression, increases abundance2
Acroleinincreases abundance, affects cotreatment, decreases expression2
Ozoneincreases abundance, affects cotreatment, decreases expression2
Phenylmercuric Acetateaffects cotreatment, decreases expression2
TAK-243increases sumoylation1
methylmercuric chlorideincreases expression1
triphenyl phosphateaffects expression1
alpha-pineneaffects cotreatment, decreases expression, increases abundance1
bisphenol Aaffects cotreatment, increases methylation1
avobenzoneincreases expression1
perfluorooctane sulfonic aciddecreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
dorsomorphinaffects cotreatment, decreases expression1
bisphenol Saffects cotreatment, increases methylation1
jinfukangdecreases expression1
Fulvestrantaffects cotreatment, increases methylation1
Air Pollutantsaffects cotreatment, decreases expression, increases abundance1
Benzo(a)pyreneincreases methylation1
Estradiolaffects cotreatment, increases expression1
Ethyl Methanesulfonateincreases expression1
Formaldehydedecreases expression1
Methyl Methanesulfonateincreases expression1
Thiramincreases expression1
Tobacco Smoke Pollutiondecreases expression1
Urethaneincreases expression1
Permethrindecreases expression1
Volatile Organic Compoundsdecreases expression, affects cotreatment1

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.