ZNF852

gene
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Summary

ZNF852 (zinc finger protein 852, HGNC:27713) is a protein-coding gene on chromosome 3p21.31, encoding Zinc finger protein 852 (Q6ZMS4). 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 285346 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 2 total

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:27713
Approved symbolZNF852
Namezinc finger protein 852
Location3p21.31
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000178917
Ensembl biotypeprotein_coding
Entrez285346

Gene structure

Transcript identifiers

Ensembl transcripts: 7 — 5 protein_coding, 1 retained_intron, 1 protein_coding_CDS_not_defined

ENST00000436261, ENST00000463067, ENST00000489411, ENST00000650400, ENST00000710690, ENST00000710691, ENST00000715584

RefSeq mRNA: 4 — MANE Select: None NM_001287349, NM_001423469, NM_001423470, NM_001423484

Canonical transcript exons

ENST00000436261 — 5 exons

ExonStartEnd
ENSE000012126594451055344510617
ENSE000017783544449176644499299
ENSE000022987714450296544503056
ENSE000036081204450254244502668
ENSE000040272884449930244500634

Expression profiles

Bgee: expression breadth ubiquitous, 134 present calls, max score 80.69.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.6124 / max 116.6307, expressed in 1431 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
418594.35941416
418580.207776
418570.045315

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.69gold quality
colonic epitheliumUBERON:000039779.84gold quality
tonsilUBERON:000237279.45gold quality
islet of LangerhansUBERON:000000677.87gold quality
monocyteCL:000057677.27gold quality
bone marrow cellCL:000209277.21gold quality
endometriumUBERON:000129576.96gold quality
leukocyteCL:000073876.90gold quality
pancreasUBERON:000126476.77gold quality
body of pancreasUBERON:000115076.25gold quality
bone marrowUBERON:000237175.08gold quality
rectumUBERON:000105274.79gold quality
lymph nodeUBERON:000002974.20gold quality
vermiform appendixUBERON:000115473.72gold quality
ganglionic eminenceUBERON:000402373.53gold quality
calcaneal tendonUBERON:000370173.32gold quality
smooth muscle tissueUBERON:000113573.08gold quality
cortical plateUBERON:000534372.59gold quality
stomachUBERON:000094572.46gold quality
duodenumUBERON:000211472.28gold quality
sural nerveUBERON:001548871.95gold quality
urinary bladderUBERON:000125571.94gold quality
adrenal tissueUBERON:001830371.81gold quality
body of stomachUBERON:000116171.79gold quality
skeletal muscle tissueUBERON:000113471.76gold quality
stromal cell of endometriumCL:000225571.71gold quality
muscle tissueUBERON:000238571.64gold quality
ovaryUBERON:000099270.99gold quality
saliva-secreting glandUBERON:000104470.84gold quality
myometriumUBERON:000129670.83gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.84

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • Zinc finger protein 852 is essential for the proliferation, drug sensitivity, and self-renewal of gastric cancer cells. (PMID:34957631)

Cross-species orthologs

0 orthologs

Paralogs (51): WIZ (ENSG00000011451), ZNF416 (ENSG00000083817), MYNN (ENSG00000085274), PRDM4 (ENSG00000110851), PRDM2 (ENSG00000116731), ZBTB17 (ENSG00000116809), ZNF644 (ENSG00000122482), GZF1 (ENSG00000125812), ZNF426 (ENSG00000130818), ZNF287 (ENSG00000141040), ZNF697 (ENSG00000143067), ZNF687 (ENSG00000143373), ZNF214 (ENSG00000149050), ZNF547 (ENSG00000152433), ZNF776 (ENSG00000152443), ZNF230 (ENSG00000159882), ZNF222 (ENSG00000159885), ZNF233 (ENSG00000159915), ZNF333 (ENSG00000160961), ZNF319 (ENSG00000166188), ZNF592 (ENSG00000166716), ZNF646 (ENSG00000167395), ZNF507 (ENSG00000168813), ZNF768 (ENSG00000169957), ZNF417 (ENSG00000173480), ZNF408 (ENSG00000175213), ZBTB41 (ENSG00000177888), ZNF223 (ENSG00000178386), ZNF784 (ENSG00000179922), ZNF572 (ENSG00000180938), ZNF707 (ENSG00000181135), ZNF746 (ENSG00000181220), ZNF467 (ENSG00000181444), ZNF530 (ENSG00000183647), ZNF17 (ENSG00000186272), ZNF527 (ENSG00000189164), ZKSCAN7 (ENSG00000196345), ZNF34 (ENSG00000196378), ZNF774 (ENSG00000196391), ZNF777 (ENSG00000196453)

Protein

Protein identifiers

Zinc finger protein 852Q6ZMS4 (reviewed: Q6ZMS4)

All UniProt accessions (5): A0A3B3ISA9, A0AA34QVT6, A0AAQ5BIJ2, A0AAQ5BIJ6, Q6ZMS4

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 (4): NP_001274278, NP_001410398, NP_001410399, NP_001410413 (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050758Znf_C2H2-typeFamily

Pfam: PF00096, PF01352

UniProt features (16 total): zinc finger region 12, chain 1, domain 1, modified residue 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6ZMS4-F170.850.52

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 (1): 145

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 20 (showing top): OSMAN_BLADDER_CANCER_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, chr3p21, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, RBM34_TARGET_GENES, MIR3685, GSE11864_UNTREATED_VS_CSF1_IFNG_PAM3CYS_IN_MAC_UP, MIR1248, MIR7973, DESCARTES_FETAL_KIDNEY_MEGAKARYOCYTES, HDGF_TARGET_GENES, ZNF394_TARGET_GENES, OSMAN_BLOOD_CHAD63_KH_AGE_18_50YO_HIGH_DOSE_SUBJECTS_24HR_DN, GOMF_DNA_BINDING_TRANSCRIPTION_FACTOR_ACTIVITY, GOMF_CIS_REGULATORY_REGION_SEQUENCE_SPECIFIC_DNA_BINDING

GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (5): 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), 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
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

136 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF852CDCP2Q5VXM1697
ZNF852NKAPLQ5M9Q1396
ZNF852METTL6Q8TCB7349
ZNF852CMTM8Q8IZV2348
ZNF852KAT8Q9H7Z6316
ZNF852CAPN7Q9Y6W3311
ZNF852VENTXO95231307
ZNF852SLC25A38Q96DW6298
ZNF852PGBD1Q96JS3283
ZNF852RPE65Q16518281
ZNF852GZMKP49863262
ZNF852BBOF1Q8ND07248
ZNF852SNRKQ9NRH2245
ZNF852LIMD1Q9UGP4224
ZNF852AADACL3Q5VUY0223
ZNF852SH3BP5O60239223

IntAct

14 interactions, top by confidence:

ABTypeScore
PRICKLE3SIAH2psi-mi:“MI:0914”(association)0.530
ARIH1SPOPpsi-mi:“MI:0914”(association)0.530
DRICH1CSNK1Epsi-mi:“MI:0914”(association)0.530
TIMM50ZNF724psi-mi:“MI:0914”(association)0.530
TIMM50ZNF724psi-mi:“MI:0914”(association)0.350
CD6CIBAR1psi-mi:“MI:0914”(association)0.350
SHISA3ZNF316psi-mi:“MI:0914”(association)0.350
PTX3POLRMTpsi-mi:“MI:0914”(association)0.350
ARIH1PHGDHpsi-mi:“MI:0914”(association)0.350
OR52B2PCCApsi-mi:“MI:0914”(association)0.350
TIMM50ZNF320psi-mi:“MI:0914”(association)0.350

BioGRID (13): ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (Affinity Capture-MS), ZNF852 (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: A2T7D2, Q01793, Q49A33, Q6GQR8, Q6ZMS4, Q86XU0, Q9P0L1, Q9Y2L8, O14709, P51523, Q32M78, Q4R6J4, Q5T5D7, A1YEP8, A1YEQ3, A1YEV9, A1YFW2, A1YFW6, A1YG26, A1YG48, A1YG60, A1YGJ4, A1YGK6, A2T6E3, A2T6V8, A2T6W2, A2T712, A2T736, A2T7D7, A2T7F2, A2T7F4, A2T7L7, A2T812, A6QNZ0, A6QPT6, B2KFW1, O14771, O14978, O15535, O43309

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

630 predictions. Top by Δscore:

VariantEffectΔscore
3:44502536:CATTA:Cdonor_loss0.9900
3:44502537:ATTAC:Adonor_loss0.9900
3:44502538:TTACC:Tdonor_loss0.9900
3:44502539:TACC:Tdonor_loss0.9900
3:44502540:ACCC:Adonor_loss0.9900
3:44502556:C:CTdonor_gain0.9900
3:44502557:T:TTdonor_gain0.9900
3:44503823:CAG:Cdonor_gain0.9900
3:44510552:CCGA:Cdonor_gain0.9900
3:44500642:C:CTacceptor_gain0.9800
3:44500643:A:Tacceptor_gain0.9800
3:44503052:TTGAG:Tacceptor_gain0.9800
3:44503057:C:CCacceptor_gain0.9800
3:44510551:A:ACdonor_gain0.9800
3:44510552:C:CCdonor_gain0.9800
3:44500635:CTG:Cacceptor_gain0.9700
3:44500642:C:Tacceptor_gain0.9700
3:44502540:AC:Adonor_gain0.9700
3:44502541:CC:Cdonor_gain0.9700
3:44502568:T:Adonor_gain0.9700
3:44503054:GAGC:Gacceptor_loss0.9600
3:44503055:AGC:Aacceptor_loss0.9600
3:44503056:GC:Gacceptor_loss0.9600
3:44503057:CTGA:Cacceptor_loss0.9600
3:44503058:T:Gacceptor_loss0.9600
3:44503053:TGAG:Tacceptor_gain0.9500
3:44507877:G:Cdonor_gain0.9500
3:44510485:CCTCA:Cdonor_loss0.9400
3:44510486:CTCAC:Cdonor_loss0.9400
3:44510487:TCAC:Tdonor_loss0.9400

AlphaMissense

3644 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:44499349:A:CF476L0.997
3:44499349:A:TF476L0.997
3:44499351:A:GF476L0.997
3:44499433:G:CF448L0.995
3:44499433:G:TF448L0.995
3:44499435:A:GF448L0.995
3:44499517:G:CF420L0.995
3:44499517:G:TF420L0.995
3:44499519:A:GF420L0.995
3:44499601:G:CF392L0.995
3:44499601:G:TF392L0.995
3:44499603:A:GF392L0.995
3:44500021:A:CF252L0.995
3:44500021:A:TF252L0.995
3:44500023:A:GF252L0.995
3:44499769:G:CF336L0.994
3:44499769:G:TF336L0.994
3:44499771:A:GF336L0.994
3:44500189:G:CF196L0.994
3:44500189:G:TF196L0.994
3:44500191:A:GF196L0.994
3:44499488:T:GQ430P0.993
3:44499685:G:CF364L0.993
3:44499685:G:TF364L0.993
3:44499687:A:GF364L0.993
3:44499404:T:GQ458P0.991
3:44499500:A:GL426P0.991
3:44499937:A:CF280L0.991
3:44499937:A:TF280L0.991
3:44499939:A:GF280L0.991

dbSNP variants (sampled 300 via entrez): RS1000038171 (3:44508155 T>G), RS1000159271 (3:44495139 A>C,G), RS1000269225 (3:44501876 G>A), RS1000414583 (3:44512365 A>G), RS1000543185 (3:44493756 G>A), RS1000866969 (3:44507286 T>C), RS1000973999 (3:44500726 A>C), RS1001005130 (3:44500318 TA>T), RS1001007372 (3:44499827 T>A,C), RS1001154068 (3:44511703 G>A), RS1001164411 (3:44493401 G>A,T), RS1001394809 (3:44505035 A>G), RS1001915218 (3:44510736 C>A,G), RS1001958231 (3:44498353 G>A), RS1002185539 (3:44491889 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

11 total (human), top 11 by PubMed support.

ChemicalActions (top 5)PubMed papers
triphenyl phosphateaffects expression1
bisphenol Aincreases expression1
tris(2-butoxyethyl) phosphateaffects expression1
sodium arseniteincreases abundance, increases expression, affects cotreatment1
manganese chlorideincreases abundance, increases expression, affects cotreatment1
Leflunomideincreases expression1
Air Pollutantsincreases expression, increases abundance1
Arsenicaffects cotreatment, increases abundance, increases expression1
Manganeseaffects cotreatment, increases abundance, increases expression1
Urethaneincreases expression1
Particulate Matterincreases abundance, increases 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.