ZNF860

gene
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Summary

ZNF860 (zinc finger protein 860, HGNC:34513) is a protein-coding gene on chromosome 3p24.1, encoding Zinc finger protein 860 (A6NHJ4). 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 344787 — RefSeq curated summary.

At a glance

  • GWAS associations: 3
  • MANE Select transcript: NM_001137674

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:34513
Approved symbolZNF860
Namezinc finger protein 860
Location3p24.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000197385
Ensembl biotypeprotein_coding
Entrez344787

Gene structure

Transcript identifiers

Ensembl transcripts: 4 — 3 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000360311, ENST00000489408, ENST00000912157, ENST00000912158

RefSeq mRNA: 1 — MANE Select: NM_001137674 NM_001137674

CCDS: CCDS46784

Canonical transcript exons

ENST00000360311 — 2 exons

ExonStartEnd
ENSE000014023663198866031991723
ENSE000017403013198175031981902

Expression profiles

Bgee: expression breadth ubiquitous, 121 present calls, max score 74.75.

FANTOM5 (CAGE): breadth broad, TPM avg 2.0893 / max 117.9256, expressed in 580 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
358672.0893580

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047374.75gold quality
cortical plateUBERON:000534373.28gold quality
lymph nodeUBERON:000002971.43gold quality
islet of LangerhansUBERON:000000668.90gold quality
calcaneal tendonUBERON:000370168.71gold quality
tonsilUBERON:000237268.01gold quality
endometriumUBERON:000129567.90gold quality
lower esophagus mucosaUBERON:003583467.39gold quality
esophagus mucosaUBERON:000246966.87gold quality
placentaUBERON:000198766.21gold quality
vermiform appendixUBERON:000115465.72gold quality
quadriceps femorisUBERON:000137765.49gold quality
urinary bladderUBERON:000125565.05gold quality
thymusUBERON:000237064.75silver quality
cerebellar vermisUBERON:000472064.61gold quality
rectumUBERON:000105263.49gold quality
smooth muscle tissueUBERON:000113563.37gold quality
olfactory segment of nasal mucosaUBERON:000538662.72gold quality
minor salivary glandUBERON:000183062.59gold quality
saliva-secreting glandUBERON:000104462.17gold quality
prostate glandUBERON:000236761.93gold quality
metanephros cortexUBERON:001053361.54gold quality
spleenUBERON:000210661.05gold quality
pituitary glandUBERON:000000761.04gold quality
adenohypophysisUBERON:000219661.03gold quality
cortex of kidneyUBERON:000122560.79gold quality
adult mammalian kidneyUBERON:000008260.36gold quality
bone marrow cellCL:000209260.27silver quality
kidneyUBERON:000211360.26gold quality
fallopian tubeUBERON:000388959.65gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.42

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): STAT1

miRNA regulators (miRDB)

48 targeting ZNF860, 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-3134100.0066.43777
HSA-MIR-548AJ-3P99.9673.385345
HSA-MIR-548X-3P99.9673.385345
HSA-MIR-4666A-3P99.9671.713434
HSA-MIR-128-3P99.9571.172484
HSA-MIR-216A-3P99.9571.192505
HSA-MIR-548J-3P99.9472.614881
HSA-MIR-548AE-3P99.9372.664867
HSA-MIR-548AH-3P99.9372.544872
HSA-MIR-548AM-3P99.9372.544872
HSA-MIR-548AQ-3P99.9372.664867
HSA-MIR-335-3P99.9373.364958
HSA-MIR-450B-5P99.9271.483175
HSA-MIR-3681-3P99.8870.462254
HSA-MIR-10395-5P99.8667.35676
HSA-MIR-5582-3P99.8672.484221
HSA-MIR-469899.8471.414303
HSA-MIR-3121-3P99.8271.963630
HSA-MIR-128399.6972.423009
HSA-MIR-58799.6470.862611
HSA-MIR-4728-3P99.4768.94981
HSA-MIR-4762-3P99.4369.722363
HSA-MIR-19A-5P99.3666.931675
HSA-MIR-19B-1-5P99.3667.071669
HSA-MIR-19B-2-5P99.3667.071669
HSA-MIR-155-5P99.3570.161509
HSA-MIR-2115-3P99.3169.682026
HSA-MIR-580-5P99.2870.941776
HSA-MIR-410-3P99.2769.982457
HSA-MIR-397899.2468.392201

Literature-anchored findings (GeneRIF, showing 1)

  • The gastric cancer (GC) tissues had significantly upregulated ZNF860 expression. High ZNF860 RNA expression was independently associated with shorter recurrence-free survival in patients with early GC. Six genes (OSBPL10, FAM208A, TOPBP1, SPTY2D1, NAB1, and CMTM6) were positively co-expressed with ZNF860, suggesting that ZNF860 probably acts as a transcription enhancer in GC. (PMID:30767193)

Cross-species orthologs

0 orthologs

Paralogs (11): ZNF761 (ENSG00000160336), ZNF701 (ENSG00000167562), ZNF816 (ENSG00000180257), ZNF766 (ENSG00000196214), ZNF765 (ENSG00000196417), ZNF813 (ENSG00000198346), ZNF525 (ENSG00000203326), ZNF468 (ENSG00000204604), ZNF888 (ENSG00000213793), ZNF578 (ENSG00000258405), (ENSG00000269825)

Protein

Protein identifiers

Zinc finger protein 860A6NHJ4 (reviewed: A6NHJ4)

All UniProt accessions (1): A6NHJ4

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_001131146* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (19 total): zinc finger region 14, sequence conflict 2, chain 1, domain 1, cross-link 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NHJ4-F163.660.01

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): 220

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 36 (showing top): GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, BARX1_TARGET_GENES, CREB3L4_TARGET_GENES, GREB1_TARGET_GENES, HMG20B_TARGET_GENES, HOXB4_TARGET_GENES, HOXC6_TARGET_GENES, ZNF2_TARGET_GENES, ZNF513_TARGET_GENES, MIR5582_3P, MIR4698, MIR2115_3P, MIR580_5P, MIR3978

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

268 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF860OR4F6Q8NGB9621
ZNF860LRRC58Q96CX6541
ZNF860OSBPL10Q9BXB5507
ZNF860MAMLD1Q13495473
ZNF860OR52E4Q8NGH9432
ZNF860CAND2O75155392
ZNF860MED8Q96G25387
ZNF860TOPAZ1Q8N9V7375
ZNF860RBM44Q6ZP01375
ZNF860SPTY2D1Q68D10375
ZNF860KIAA1328Q86T90370
ZNF860TAFA4Q96LR4370
ZNF860LPGAT1Q92604369
ZNF860MOB3CQ70IA8366
ZNF860ACAD10Q6JQN1349

IntAct

7 interactions, top by confidence:

ABTypeScore
ZNF860CEP70psi-mi:“MI:0915”(physical association)0.560
ZNF860KRTAP10-9psi-mi:“MI:0915”(physical association)0.560
ZNF860CEP70psi-mi:“MI:0915”(physical association)0.000
ZNF860KRTAP10-9psi-mi:“MI:0915”(physical association)0.000
CEP70ZNF860psi-mi:“MI:0915”(physical association)0.000

BioGRID (4): ZNF860 (Affinity Capture-RNA), ZNF860 (Affinity Capture-RNA), ZNF860 (Two-hybrid), KRTAP10-9 (Two-hybrid)

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, A2RRD8, A2VDQ7, A6NHJ4, A6NK75, A6NN14, A6NNF4, A6NP11, B4DX44, B4DXR9, E9PW05, O14628, O43345, O75290, O75346, O75373, O75820, P0CB33, P0CJ79, P0DKX0, P10755, P17032, P17035, P52738, Q02386, Q03923, Q03936, Q05481, Q08AN1, Q09FC8, Q0VGE8, Q14586, Q14593, Q147U1, Q15928, Q3MIS6, Q3SXZ3, Q494X3, Q4R6C2, Q5HY98

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

98 predictions. Top by Δscore:

VariantEffectΔscore
3:31981850:G:Tdonor_gain0.9900
3:31981900:CAGG:Cdonor_loss0.9900
3:31981901:AGGT:Adonor_loss0.9900
3:31981903:GTA:Gdonor_loss0.9900
3:31983081:GCCA:Gdonor_gain0.9900
3:31983087:T:Adonor_gain0.9800
3:31981903:G:GGdonor_gain0.9700
3:31981849:G:GTdonor_gain0.9600
3:31983084:A:AGdonor_gain0.9600
3:31983085:G:GGdonor_gain0.9600
3:31981893:A:AGdonor_gain0.9400
3:31981880:G:Tdonor_gain0.9300
3:31988658:A:AGacceptor_gain0.8400
3:31988659:G:GGacceptor_gain0.8400
3:31988659:GTCA:Gacceptor_gain0.8400
3:31988659:GT:Gacceptor_gain0.8300
3:31988658:A:Tacceptor_gain0.8100
3:31988654:CATCA:Cacceptor_gain0.8000
3:31988655:ATCAG:Aacceptor_gain0.7900
3:31988656:TCAGT:Tacceptor_gain0.7900
3:31988657:CAG:Cacceptor_gain0.7900
3:31988659:GTC:Gacceptor_gain0.7800
3:31988653:T:Gacceptor_gain0.7700
3:31988659:G:Tacceptor_gain0.7700
3:31988652:A:AGacceptor_gain0.7600
3:31986236:T:Gacceptor_gain0.7500
3:31981894:T:Gdonor_gain0.7400
3:31981900:CAG:Cdonor_gain0.7400
3:31988658:A:ACacceptor_loss0.6900
3:31988659:G:Aacceptor_loss0.6900

AlphaMissense

4262 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
3:31990214:T:CF379L0.996
3:31990216:T:AF379L0.996
3:31990216:T:GF379L0.996
3:31990466:T:CF463L0.995
3:31990468:C:AF463L0.995
3:31990468:C:GF463L0.995
3:31990130:T:CF351L0.994
3:31990132:C:AF351L0.994
3:31990132:C:GF351L0.994
3:31990046:T:CF323L0.993
3:31990048:T:AF323L0.993
3:31990048:T:GF323L0.993
3:31990416:G:CR446P0.993
3:31990550:T:CF491L0.993
3:31990552:C:AF491L0.993
3:31990552:C:GF491L0.993
3:31990137:G:CR353P0.986
3:31990493:C:GH472D0.986
3:31990634:T:CF519L0.985
3:31990636:T:AF519L0.985
3:31990636:T:GF519L0.985
3:31989962:T:CF295L0.984
3:31989964:T:AF295L0.984
3:31989964:T:GF295L0.984
3:31990159:C:AH360Q0.982
3:31990159:C:GH360Q0.982
3:31990485:T:CL469P0.981
3:31990493:C:AH472N0.980
3:31990725:G:CR549P0.980
3:31990389:G:CR437P0.979

dbSNP variants (sampled 300 via entrez): RS1000035986 (3:32000455 A>G), RS1000156100 (3:31994646 T>C,G), RS1000298873 (3:31986028 T>C), RS1000374836 (3:31980699 G>A), RS1000405524 (3:32000778 C>A,T), RS1000412357 (3:31980557 C>A), RS1000504620 (3:32000525 A>G), RS1000505626 (3:31982711 A>G), RS1000736976 (3:32005620 A>G,T), RS1000830435 (3:32005794 A>G), RS1000902423 (3:31988606 C>G,T), RS1001103977 (3:31992734 C>G), RS1001118391 (3:31994517 G>A), RS1001119364 (3:32006851 C>T), RS1001344196 (3:32003949 G>A,C)

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

3 associations (top):

StudyTraitp-value
GCST002312_8Periodontal disease-related phenotype (Socransky)6.000000e-06
GCST004946_13Schizophrenia3.000000e-08
GCST012174_1Diabetic retinopathy in type 2 diabetes7.000000e-10

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

13 total (human), top 13 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, increases expression2
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
ethyl-p-hydroxybenzoateincreases expression1
nutlin 3affects cotreatment, increases expression1
abrinedecreases expression1
licochalcone Bdecreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acidincreases expression1
Temozolomidedecreases expression1
Dactinomycinaffects cotreatment, increases expression1
Smokeincreases expression1
Urethanedecreases expression1
Aflatoxin B1decreases methylation1

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): diabetic retinopathy