ZNF765

gene
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Summary

ZNF765 (zinc finger protein 765, HGNC:25092) is a protein-coding gene on chromosome 19q13.42, encoding Zinc finger protein 765 (Q7L2R6). 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 91661 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 92 total
  • MANE Select transcript: NM_001040185

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25092
Approved symbolZNF765
Namezinc finger protein 765
Location19q13.42
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000196417
Ensembl biotypeprotein_coding
Entrez91661

Gene structure

Transcript identifiers

Ensembl transcripts: 10 — 5 protein_coding, 3 protein_coding_CDS_not_defined, 2 nonsense_mediated_decay

ENST00000396408, ENST00000504146, ENST00000504235, ENST00000505866, ENST00000507045, ENST00000594030, ENST00000594627, ENST00000596086, ENST00000933978, ENST00000963919

RefSeq mRNA: 2 — MANE Select: NM_001040185 NM_001040185, NM_001350495

CCDS: CCDS46171

Canonical transcript exons

ENST00000396408 — 4 exons

ExonStartEnd
ENSE000015248255340769853412009
ENSE000020552625339514953395193
ENSE000032836385340206553402191
ENSE000035571755339794353398030

Expression profiles

Bgee: expression breadth ubiquitous, 246 present calls, max score 90.92.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.3438 / max 57.4145, expressed in 1190 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1773256.14891654
1773243.34381190

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
oocyteCL:000002390.92gold quality
germinal epithelium of ovaryUBERON:000130490.50gold quality
secondary oocyteCL:000065589.75gold quality
thymusUBERON:000237087.80gold quality
epithelium of nasopharynxUBERON:000195187.75gold quality
palpebral conjunctivaUBERON:000181284.54gold quality
mucosa of paranasal sinusUBERON:000503084.18gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.52gold quality
adrenal tissueUBERON:001830382.52gold quality
jejunal mucosaUBERON:000039982.37gold quality
mucosa of sigmoid colonUBERON:000499382.12gold quality
parietal pleuraUBERON:000240081.56gold quality
amniotic fluidUBERON:000017381.37gold quality
tibiaUBERON:000097981.21gold quality
colonic mucosaUBERON:000031781.10gold quality
visceral pleuraUBERON:000240180.94gold quality
gingival epitheliumUBERON:000194980.84gold quality
lower lobe of lungUBERON:000894980.84gold quality
placentaUBERON:000198780.69gold quality
ganglionic eminenceUBERON:000402380.24gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.08gold quality
ovaryUBERON:000099279.97gold quality
trabecular bone tissueUBERON:000248379.57gold quality
calcaneal tendonUBERON:000370179.54gold quality
esophagus squamous epitheliumUBERON:000692079.54gold quality
oral cavityUBERON:000016779.46gold quality
right adrenal gland cortexUBERON:003582779.23gold quality
gingivaUBERON:000182879.00gold quality
bone marrowUBERON:000237178.89gold quality
islet of LangerhansUBERON:000000678.87gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes6.69

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • IGF2BP2 stabilized FBXL19-AS1 regulates the blood-tumour barrier permeability by negatively regulating ZNF765 by STAU1-mediated mRNA decay. (PMID:32713259)

Cross-species orthologs

0 orthologs

Paralogs (11): ZNF761 (ENSG00000160336), ZNF701 (ENSG00000167562), ZNF816 (ENSG00000180257), ZNF766 (ENSG00000196214), ZNF860 (ENSG00000197385), ZNF813 (ENSG00000198346), ZNF525 (ENSG00000203326), ZNF468 (ENSG00000204604), ZNF888 (ENSG00000213793), ZNF578 (ENSG00000258405), (ENSG00000269825)

Protein

Protein identifiers

Zinc finger protein 765Q7L2R6 (reviewed: Q7L2R6)

All UniProt accessions (3): Q7L2R6, D6RF03, E9PDE6

UniProt curated annotations — full annotation on UniProt →

Function. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.

Similarity. Belongs to the krueppel C2H2-type zinc-finger protein family.

Isoforms (3)

UniProt IDNamesCanonical?
Q7L2R6-11yes
Q7L2R6-22
Q7L2R6-33

RefSeq proteins (2): NP_001035275, NP_001337424 (=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 (25 total): zinc finger region 11, sequence conflict 6, splice variant 4, chain 1, domain 1, cross-link 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q7L2R6-F163.840.04

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): 205

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-9843940Regulation of endogenous retroelements by KRAB-ZFP proteins

MSigDB gene sets: 66 (showing top): LIAO_METASTASIS, MODULE_544, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, JOHNSTONE_PARVB_TARGETS_3_DN, MODULE_481, REACTOME_EPIGENETIC_REGULATION_OF_GENE_EXPRESSION, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ELF2_TARGET_GENES, ZNF350_TARGET_GENES, MIR616_5P, MIR371B_5P, MIR373_5P, MIR4698, MIR23A_3P_MIR23B_3P, MIR23C

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 (2): nucleus (GO:0005634), nuclear lumen (GO:0031981)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
Regulation of endogenous retroelements1

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
nucleus1
intracellular organelle lumen1

Protein interactions and networks

STRING

484 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF765FAAH2Q6GMR7525
ZNF765PDXDC1Q6P996516
ZNF765PDHBP11177359
ZNF765VOPP1Q96AW1322
ZNF765STAU1O95793305
ZNF765ADAP1O75689299
ZNF765BAIAP3O94812277
ZNF765ABHD3Q8WU67276
ZNF765N4BP2L2Q92802269
ZNF765ENOPH1Q9UHY7267
ZNF765CEP295Q9C0D2263
ZNF765HOOK2Q96ED9251
ZNF765MED11Q9P086250
ZNF765C9orf153Q5TBE3248
ZNF765RAX2Q96IS3248

IntAct

22 interactions, top by confidence:

ABTypeScore
ZNF765TRIM28psi-mi:“MI:0915”(physical association)0.620
ZNF765RELpsi-mi:“MI:0915”(physical association)0.560
DZIP3ZNF765psi-mi:“MI:0915”(physical association)0.560
USHBP1ZNF765psi-mi:“MI:0915”(physical association)0.560
RELZNF765psi-mi:“MI:0915”(physical association)0.560
ZNF765DZIP3psi-mi:“MI:0915”(physical association)0.560
ZNF765USHBP1psi-mi:“MI:0915”(physical association)0.560
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ZNF765IPO7psi-mi:“MI:0915”(physical association)0.500
taxZNF765psi-mi:“MI:0915”(physical association)0.490
ZNF765taxpsi-mi:“MI:0915”(physical association)0.490
Mpsi-mi:“MI:0914”(association)0.350
ZNF765TRIM24psi-mi:“MI:0914”(association)0.350
ZNF467ZNF320psi-mi:“MI:0914”(association)0.350
FBLN5ZNF320psi-mi:“MI:0914”(association)0.350
NOTCH2ZNF320psi-mi:“MI:0914”(association)0.350
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
CUL9NVLpsi-mi:“MI:0914”(association)0.350

BioGRID (23): ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Affinity Capture-MS), ZNF765 (Affinity Capture-RNA), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ZNF765 (Two-hybrid), ARID5A (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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance81
Likely benign5
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

679 predictions. Top by Δscore:

VariantEffectΔscore
19:53395190:GCGG:Gdonor_gain1.0000
19:53395192:GG:Gdonor_gain1.0000
19:53395192:GGGTG:Gdonor_loss1.0000
19:53395193:GG:Gdonor_gain1.0000
19:53395194:G:GAdonor_loss1.0000
19:53395194:G:GGdonor_gain1.0000
19:53395195:T:Adonor_loss1.0000
19:53402152:G:Tdonor_gain1.0000
19:53395189:CGCGG:Cdonor_gain0.9900
19:53395190:GCGGG:Gdonor_gain0.9900
19:53395191:CGG:Cdonor_gain0.9900
19:53395192:GGG:Gdonor_gain0.9900
19:53398029:AGGT:Adonor_loss0.9900
19:53398030:GGTGA:Gdonor_loss0.9900
19:53398031:G:GAdonor_loss0.9900
19:53398032:T:Gdonor_loss0.9900
19:53397940:CA:Cacceptor_loss0.9800
19:53397941:A:AGacceptor_gain0.9800
19:53397942:G:GGacceptor_gain0.9800
19:53397942:GGATT:Gacceptor_gain0.9800
19:53402190:GG:Gdonor_gain0.9800
19:53402191:GG:Gdonor_gain0.9800
19:53402197:G:GTdonor_gain0.9800
19:53402215:G:GTdonor_gain0.9800
19:53404549:TTC:Tdonor_gain0.9800
19:53397941:AG:Aacceptor_gain0.9700
19:53397942:GG:Gacceptor_gain0.9700
19:53402152:G:GTdonor_gain0.9700
19:53402215:G:Tdonor_gain0.9700
19:53402059:T:Gacceptor_loss0.9600

AlphaMissense

3523 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:53408561:T:CF336L0.993
19:53408563:T:AF336L0.993
19:53408563:T:GF336L0.993
19:53408645:T:CF364L0.990
19:53408647:T:AF364L0.990
19:53408647:T:GF364L0.990
19:53408729:T:CF392L0.989
19:53408731:T:AF392L0.989
19:53408731:T:GF392L0.989
19:53408393:T:CF280L0.988
19:53408395:C:AF280L0.988
19:53408395:C:GF280L0.988
19:53408477:T:CF308L0.985
19:53408479:C:AF308L0.985
19:53408479:C:GF308L0.985
19:53408978:T:CF475L0.983
19:53408980:C:AF475L0.983
19:53408980:C:GF475L0.983
19:53408652:G:CR366P0.975
19:53408580:T:CL342P0.974
19:53409062:T:CF503L0.968
19:53409064:C:AF503L0.968
19:53409064:C:GF503L0.968
19:53402089:G:CA14P0.967
19:53408588:C:GH345D0.967
19:53402098:T:CF17L0.964
19:53402100:C:AF17L0.964
19:53402100:C:GF17L0.964
19:53408562:T:CF336S0.963
19:53408590:T:AH345Q0.963

dbSNP variants (sampled 300 via entrez): RS1000217926 (19:53414615 T>G), RS1000246805 (19:53398593 T>C), RS1000273355 (19:53414189 C>G,T), RS1000380595 (19:53419529 G>A,T), RS1000445332 (19:53425132 C>G,T), RS1000472790 (19:53417100 G>A,T), RS1000563417 (19:53413201 T>A,C), RS1000615744 (19:53413001 T>C), RS1000672592 (19:53418626 G>A,C), RS1000769842 (19:53423890 C>T), RS1000822298 (19:53423497 C>T), RS1001008866 (19:53419925 A>G), RS1001127224 (19:53418442 C>T), RS1001132975 (19:53398437 G>A), RS1001277612 (19:53415525 T>G)

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

17 total (human), top 17 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyrenedecreases methylation, increases expression2
GSK-J4decreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
avobenzonedecreases expression1
di-n-butylphosphoric acidaffects expression1
jinfukangdecreases expression1
Air Pollutantsdecreases expression, increases abundance1
Succimeraffects cotreatment, increases expression1
Doxorubicindecreases expression1
Ethyl Methanesulfonateincreases expression1
Methyl Methanesulfonateincreases expression1
Smokedecreases expression1
Tobacco Smoke Pollutionincreases expression1
Valproic Acidincreases expression1
Particulate Matterdecreases expression, increases abundance1
Magnetite Nanoparticlesaffects cotreatment, 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.