ZNF785

gene
On this page

Also known as FLJ32130

Summary

ZNF785 (zinc finger protein 785, HGNC:26496) is a protein-coding gene on chromosome 16p11.2, encoding Zinc finger protein 785 (A8K8V0). 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 active in nucleus.

Source: NCBI Gene 146540 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 56 total
  • MANE Select transcript: NM_152458

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26496
Approved symbolZNF785
Namezinc finger protein 785
Location16p11.2
Locus typegene with protein product
StatusApproved
AliasesFLJ32130
Ensembl geneENSG00000197162
Ensembl biotypeprotein_coding
Entrez146540

Gene structure

Transcript identifiers

Ensembl transcripts: 10 — 9 protein_coding, 1 nonsense_mediated_decay

ENST00000395216, ENST00000470110, ENST00000562128, ENST00000567773, ENST00000891565, ENST00000891566, ENST00000912832, ENST00000912833, ENST00000912834, ENST00000971000

RefSeq mRNA: 1 — MANE Select: NM_152458 NM_152458

CCDS: CCDS10685

Canonical transcript exons

ENST00000395216 — 3 exons

ExonStartEnd
ENSE000015209413058065630583443
ENSE000019255883058540730585697
ENSE000034829773058512230585250

Expression profiles

Bgee: expression breadth ubiquitous, 233 present calls, max score 93.10.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.0964 / max 53.8371, expressed in 1422 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1570722.43111057
1570711.6652893

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
buccal mucosa cellCL:000233693.10gold quality
oviduct epitheliumUBERON:000480488.15gold quality
kidney epitheliumUBERON:000481985.03gold quality
ganglionic eminenceUBERON:000402384.52gold quality
cortical plateUBERON:000534383.53gold quality
apex of heartUBERON:000209882.98gold quality
cerebellar vermisUBERON:000472082.80gold quality
cerebellar hemisphereUBERON:000224582.74gold quality
cerebellar cortexUBERON:000212982.71gold quality
cerebellumUBERON:000203782.68gold quality
right hemisphere of cerebellumUBERON:001489082.32gold quality
pylorusUBERON:000116682.09gold quality
thymusUBERON:000237081.64gold quality
cardia of stomachUBERON:000116281.57gold quality
sural nerveUBERON:001548881.49gold quality
vena cavaUBERON:000408780.98silver quality
stromal cell of endometriumCL:000225580.93gold quality
subthalamic nucleusUBERON:000190680.93gold quality
ventral tegmental areaUBERON:000269180.90gold quality
ventricular zoneUBERON:000305380.54gold quality
dorsal plus ventral thalamusUBERON:000189780.12gold quality
fallopian tubeUBERON:000388980.05gold quality
left ventricle myocardiumUBERON:000656680.04gold quality
right ovaryUBERON:000211880.03gold quality
cardiac muscle of right atriumUBERON:000337979.94gold quality
renal medullaUBERON:000036279.89gold quality
inferior vagus X ganglionUBERON:000536379.69gold quality
body of uterusUBERON:000985379.64gold quality
body of tongueUBERON:001187679.64silver quality
endocervixUBERON:000045879.62gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no4.45

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

60 targeting ZNF785, 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-3613-3P100.0076.367965
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-318599.9968.121959
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-6780A-5P99.8866.692776
HSA-MIR-30A-3P99.8769.742928
HSA-MIR-30E-3P99.8769.682942
HSA-MIR-30D-3P99.8769.922917
HSA-MIR-1273H-5P99.7766.322471
HSA-MIR-2681-5P99.7567.641655
HSA-MIR-430699.7270.503630
HSA-MIR-371499.7170.742671
HSA-MIR-30B-3P99.7065.762325
HSA-MIR-3689A-3P99.7065.732306
HSA-MIR-3689B-3P99.7065.712311
HSA-MIR-3689C99.7065.712311
HSA-MIR-6779-5P99.7065.762363
HSA-MIR-545-5P99.6670.182308
HSA-MIR-570099.6469.882280
HSA-MIR-182799.6368.573265
HSA-MIR-449999.6267.291470
HSA-MIR-427699.5667.662514
HSA-MIR-7106-5P99.5367.473574
HSA-MIR-766-3P99.4765.241811
HSA-MIR-372-5P99.4169.112299
HSA-MIR-508-5P99.4164.251248
HSA-MIR-6731-5P99.2867.422375
HSA-MIR-808599.2867.562362

Cross-species orthologs

15 orthologs

OrganismSymbolGene ID
danio_rerioznf646ENSDARG00000061424
danio_reriosi:dkey-89b17.4ENSDARG00000075545
danio_reriozgc:66472ENSDARG00000075916
danio_reriosi:ch211-148l7.4ENSDARG00000094469
danio_rerioznf576.1ENSDARG00000097819
drosophila_melanogasteraz2FBGN0025185
drosophila_melanogasterCG2129FBGN0030008
drosophila_melanogasterCG1602FBGN0033186
drosophila_melanogasterCG18011FBGN0033491
drosophila_melanogasterCG12942FBGN0033569
drosophila_melanogasterindraFBGN0035213
drosophila_melanogasterCG30020FBGN0050020
drosophila_melanogastermldFBGN0263490
caenorhabditis_elegansztf-15WBGENE00011066
caenorhabditis_elegansWBGENE00015649

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), ZNF569 (ENSG00000196437), ZNF420 (ENSG00000197050), ZNF665 (ENSG00000197497), ZNF181 (ENSG00000197841), ZNF347 (ENSG00000197937), ZNF84 (ENSG00000198040), ZBTB48 (ENSG00000204859), ZNF845 (ENSG00000213799), ZNF99 (ENSG00000213973), ZNF688 (ENSG00000229809)

Protein

Protein identifiers

Zinc finger protein 785A8K8V0 (reviewed: A8K8V0)

All UniProt accessions (3): A8K8V0, H3BR67, I3L119

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?
A8K8V0-11yes
A8K8V0-22

RefSeq proteins (1): NP_689671* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050589Ikaros_C2H2-ZFFamily

Pfam: PF00096, PF01352

UniProt features (15 total): zinc finger region 7, region of interest 2, sequence variant 2, chain 1, domain 1, compositionally biased region 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A8K8V0-F163.770.10

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 52 (showing top): chr16p11, ZHOU_INFLAMMATORY_RESPONSE_LIVE_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, HATADA_METHYLATED_IN_LUNG_CANCER_UP, MARTENS_TRETINOIN_RESPONSE_DN, ZHOU_INFLAMMATORY_RESPONSE_FIMA_DN, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ASH1L_TARGET_GENES, BARX1_TARGET_GENES, CREB3L4_TARGET_GENES, DIDO1_TARGET_GENES, E2F2_TARGET_GENES, E2F5_TARGET_GENES, HSD17B8_TARGET_GENES, KAT5_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 (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
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

Protein interactions and networks

STRING

482 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF785KIAA1958Q8N8K9425
ZNF785CCDC74BQ96LY2400
ZNF785CCDC169A6NNP5379
ZNF785CCDC190Q86UF4370
ZNF785CCDC125Q86Z20357
ZNF785RNPEPL1Q9HAU8348
ZNF785CENATACQ86UT8348
ZNF785GTF3C6Q969F1348
ZNF785ZBTB8AQ96BR9348
ZNF785CCDC171Q6TFL3318
ZNF785MOSPD3O75425311
ZNF785THAP7Q9BT49306
ZNF785AVL9Q8NBF6301
ZNF785ZSWIM4Q9H7M6299
ZNF785SLC25A45Q8N413297

IntAct

78 interactions, top by confidence:

ABTypeScore
ZNF785MTUS2psi-mi:“MI:0915”(physical association)0.670
MTUS2ZNF785psi-mi:“MI:0915”(physical association)0.670
ZNF785PNMA2psi-mi:“MI:0915”(physical association)0.670
ZNF785EHMT2psi-mi:“MI:0915”(physical association)0.560
KRTAP10-5ZNF785psi-mi:“MI:0915”(physical association)0.560
HOOK1ZNF785psi-mi:“MI:0915”(physical association)0.560
ZNF785MID2psi-mi:“MI:0915”(physical association)0.560
ZNF785psi-mi:“MI:0915”(physical association)0.560
ZNF785KRTAP10-5psi-mi:“MI:0915”(physical association)0.560
ZNF785psi-mi:“MI:0915”(physical association)0.560
ZNF785AKAP8Lpsi-mi:“MI:0915”(physical association)0.560
CABP2ZNF785psi-mi:“MI:0915”(physical association)0.560
ZNF785CCNDBP1psi-mi:“MI:0915”(physical association)0.560
ZNF785TRIP6psi-mi:“MI:0915”(physical association)0.560
ZNF785MDFIpsi-mi:“MI:0915”(physical association)0.560
ZNF785STX2psi-mi:“MI:0915”(physical association)0.560

BioGRID (152): ZNF785 (Two-hybrid), ZNF785 (Two-hybrid), ZNF785 (Two-hybrid), ZNF785 (Two-hybrid), KRTAP10-1 (Two-hybrid), KRTAP10-5 (Two-hybrid), BEND3 (Affinity Capture-MS), DOCK6 (Affinity Capture-MS), TRIO (Affinity Capture-MS), SMARCAD1 (Affinity Capture-MS), LZTS2 (Affinity Capture-MS), MTCL1 (Affinity Capture-MS), KIF7 (Affinity Capture-MS), PDZRN3 (Affinity Capture-MS), PPP2R3A (Affinity Capture-MS)

ESM2 similar proteins: A2CE44, A6NFI3, A6NM28, A8K8V0, O15370, O70218, O95201, P0CJ78, P10075, P10754, P28698, P70338, Q04890, Q07120, Q14V87, Q19A40, Q569E7, Q58DK7, Q5DWN0, Q5FWU5, Q5RJR4, Q5T619, Q5TEC3, Q6DD87, Q6IQX8, Q6PD29, Q6PGE4, Q6ZMY9, Q7Z7K2, Q80VM4, Q8BIF9, Q8JZL0, Q8N8E2, Q8NAF0, Q8NCA9, Q8TD94, Q8WUU4, Q96C55, Q96H86, Q96MX3

Diamond homologs: A1L1L7, A3KN32, A3KN36, A6NFI3, A6NM28, A6NN14, A6QLU5, A7MBI1, A8K8V0, A8MTY0, A8MWA4, B4DU55, C9JBD0, G3X9G7, O60765, O75290, O94892, O95780, P0C7X2, P10072, P15622, P16373, P16374, P17023, P17032, P17097, P17098, P21506, P52742, P59923, Q06730, Q08DG8, Q16587, Q29RZ4, Q2TL60, Q3V080, Q49AA0, Q4R6C2, Q4V8A8, Q5FWF6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance49
Likely benign2
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

512 predictions. Top by Δscore:

VariantEffectΔscore
16:30583444:C:CCacceptor_gain1.0000
16:30585107:AT:Adonor_gain1.0000
16:30585127:T:TAdonor_gain1.0000
16:30583440:GATC:Gacceptor_gain0.9900
16:30583441:ATC:Aacceptor_gain0.9900
16:30583442:TC:Tacceptor_gain0.9900
16:30583443:CC:Cacceptor_gain0.9900
16:30583443:CCTGA:Cacceptor_loss0.9900
16:30583444:CTGA:Cacceptor_loss0.9900
16:30583445:T:Cacceptor_loss0.9900
16:30583450:C:CTacceptor_gain0.9900
16:30585108:T:Cdonor_gain0.9900
16:30585363:C:Adonor_gain0.9900
16:30585401:CCTCA:Cdonor_loss0.9900
16:30585402:CTCA:Cdonor_loss0.9900
16:30585403:TCA:Tdonor_loss0.9900
16:30585404:CACCC:Cdonor_loss0.9900
16:30585405:A:Tdonor_loss0.9900
16:30585405:AC:Adonor_gain0.9900
16:30585406:CC:Cdonor_gain0.9900
16:30585445:T:TAdonor_gain0.9900
16:30585446:C:Adonor_gain0.9900
16:30583439:GGATC:Gacceptor_gain0.9800
16:30583451:A:Tacceptor_gain0.9800
16:30585107:ATC:Adonor_gain0.9800
16:30585117:AGTAC:Adonor_loss0.9800
16:30585118:GTAC:Gdonor_loss0.9800
16:30585119:TACC:Tdonor_loss0.9800
16:30585120:ACCT:Adonor_loss0.9800
16:30585121:C:Adonor_loss0.9800

AlphaMissense

2650 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:30582731:G:CF349L0.999
16:30582731:G:TF349L0.999
16:30582733:A:GF349L0.999
16:30582815:G:CF321L0.999
16:30582815:G:TF321L0.999
16:30582817:A:GF321L0.999
16:30582899:G:CF293L0.999
16:30582899:G:TF293L0.999
16:30582901:A:GF293L0.999
16:30582983:G:CF265L0.999
16:30582983:G:TF265L0.999
16:30582985:A:GF265L0.999
16:30582732:A:GF349S0.998
16:30583067:G:CF237L0.998
16:30583067:G:TF237L0.998
16:30583069:A:GF237L0.998
16:30583151:G:CF209L0.998
16:30583151:G:TF209L0.998
16:30583153:A:GF209L0.998
16:30582790:G:TH330N0.997
16:30582816:A:GF321S0.997
16:30582867:C:GR304P0.997
16:30582874:G:CH302D0.997
16:30582874:G:TH302N0.997
16:30582958:G:CH274D0.997
16:30582958:G:TH274N0.997
16:30583068:A:GF237S0.997
16:30582788:G:CH330Q0.996
16:30582788:G:TH330Q0.996
16:30582790:G:CH330D0.996

dbSNP variants (sampled 300 via entrez): RS1000474494 (16:30586463 C>T), RS1000775156 (16:30587520 C>T), RS1000780617 (16:30581816 G>A), RS1000922024 (16:30581079 G>A,C), RS1001081696 (16:30587327 C>A,G,T), RS1001234391 (16:30583181 G>A,C), RS1001752651 (16:30587661 A>C,G,T), RS1002639502 (16:30581750 C>A), RS1002953057 (16:30583854 A>C), RS1003079353 (16:30584279 A>G), RS1003724405 (16:30578026 T>C), RS1004152121 (16:30577872 G>A), RS1004245617 (16:30578151 C>T), RS1004494641 (16:30585573 G>A,C,T), RS1005074176 (16:30583709 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

1 associations (top):

StudyTraitp-value
GCST004606_92Eosinophil count2.000000e-10

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004842eosinophil count

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

18 total (human), top 18 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidincreases methylation, affects cotreatment, decreases expression, affects expression9
Panobinostataffects cotreatment, decreases expression2
Phenylmercuric Acetateaffects cotreatment, decreases expression2
TAK-243increases sumoylation1
di-n-butylphosphoric acidaffects expression1
2-palmitoylglycerolincreases 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
Benzo(a)pyrenedecreases methylation1
Coumestroldecreases expression1
Diazinonincreases methylation1
Doxorubicinincreases expression1
Phthalic Acidsdecreases methylation1
Smokedecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Cadmium Chloridedecreases expression1
Lactic Acidincreases expression1
Particulate Matterincreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_XW85HEK293 eGFP-ZNF785Transformed cell lineFemale

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.