ZNF432

gene
On this page

Also known as KIAA0798

Summary

ZNF432 (zinc finger protein 432, HGNC:20810) is a protein-coding gene on chromosome 19q13.41, encoding Zinc finger protein 432 (O94892). Homologous recombination repressor that functions as a poly(ADP-ribose) (PAR) reader regulating DNA damage response and PARP inhibition.

Enables damaged DNA binding activity and protein-macromolecule adaptor activity. Involved in DNA damage response. Located in nucleoplasm.

Source: NCBI Gene 9668 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 109 total
  • MANE Select transcript: NM_014650

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:20810
Approved symbolZNF432
Namezinc finger protein 432
Location19q13.41
Locus typegene with protein product
StatusApproved
AliasesKIAA0798
Ensembl geneENSG00000256087
Ensembl biotypeprotein_coding
OMIM620554
Entrez9668

Gene structure

Transcript identifiers

Ensembl transcripts: 8 — 7 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000221315, ENST00000594154, ENST00000597273, ENST00000598446, ENST00000598745, ENST00000600368, ENST00000601310, ENST00000913743

RefSeq mRNA: 3 — MANE Select: NM_014650 NM_001322284, NM_001322285, NM_014650

CCDS: CCDS12848

Canonical transcript exons

ENST00000221315 — 5 exons

ExonStartEnd
ENSE000011240265204685452047060
ENSE000012832225203137852035440
ENSE000015097565204869552048838
ENSE000024630485204048852040583
ENSE000025155915204148052041606

Expression profiles

Bgee: expression breadth ubiquitous, 280 present calls, max score 95.22.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 1.9136 / max 58.5584, expressed in 995 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
18251610.12731720
1825151.4143823
1825140.4993263

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
endothelial cellCL:000011595.22gold quality
pancreatic ductal cellCL:000207993.01gold quality
choroid plexus epitheliumUBERON:000391190.41gold quality
calcaneal tendonUBERON:000370189.16gold quality
hair follicleUBERON:000207387.06gold quality
body of pancreasUBERON:000115086.81gold quality
Brodmann (1909) area 23UBERON:001355486.31gold quality
cervix squamous epitheliumUBERON:000692285.95gold quality
sural nerveUBERON:001548885.60gold quality
bronchial epithelial cellCL:000232885.46gold quality
periodontal ligamentUBERON:000826685.09gold quality
tendonUBERON:000004385.07gold quality
germinal epithelium of ovaryUBERON:000130484.52gold quality
pleuraUBERON:000097784.26gold quality
parietal pleuraUBERON:000240084.19gold quality
visceral pleuraUBERON:000240184.10gold quality
epithelium of bronchusUBERON:000203183.76gold quality
oviduct epitheliumUBERON:000480483.66gold quality
epithelial cell of pancreasCL:000008383.43gold quality
ventricular zoneUBERON:000305383.33gold quality
bronchusUBERON:000218583.24gold quality
pigmented layer of retinaUBERON:000178283.22gold quality
caput epididymisUBERON:000435883.00gold quality
prostate glandUBERON:000236782.59gold quality
pancreasUBERON:000126482.57gold quality
blood vessel layerUBERON:000479782.52gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.46gold quality
ganglionic eminenceUBERON:000402382.05gold quality
tibiaUBERON:000097982.02gold quality
endometriumUBERON:000129581.60gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no4.02

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

96 targeting ZNF432, 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-7110-3P100.0073.182486
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-3925-3P100.0069.951237
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-428299.9975.366408
HSA-MIR-450099.9972.722367
HSA-LET-7A-5P99.9872.291790
HSA-LET-7B-5P99.9872.311790
HSA-LET-7C-5P99.9872.291790
HSA-LET-7E-5P99.9872.291790
HSA-LET-7F-5P99.9872.561784
HSA-LET-7G-5P99.9872.371784
HSA-LET-7I-5P99.9872.371788
HSA-MIR-98-5P99.9872.331787
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-1250-3P99.9670.044038
HSA-MIR-391099.9571.132227
HSA-MIR-141-3P99.9472.792421
HSA-MIR-200A-3P99.9472.682420
HSA-MIR-335-3P99.9373.364958
HSA-MIR-7-1-3P99.9171.534384
HSA-MIR-7-2-3P99.9171.404394
HSA-MIR-6780A-5P99.8866.692776
HSA-MIR-5003-3P99.8569.292517
HSA-MIR-4728-5P99.8569.394718
HSA-MIR-544A99.8468.661965
HSA-MIR-442099.8270.081624
HSA-MIR-6875-3P99.8270.262983
HSA-MIR-6785-5P99.8268.684428
HSA-MIR-181B-2-3P99.8170.061646

Literature-anchored findings (GeneRIF, showing 2)

  • Inhaled corticosteroids appear to modulate the association of bronchodilator response with variant(s) in the ZNF432 gene among adults and children with asthma. (PMID:24280104)
  • ZNF432 stimulates PARylation and inhibits DNA resection to balance PARPi sensitivity and resistance. (PMID:37823600)

Cross-species orthologs

0 orthologs

Paralogs (176): ZNF195 (ENSG00000005801), ZNF112 (ENSG00000062370), ZNF275 (ENSG00000063587), ZNF37A (ENSG00000075407), ZNF510 (ENSG00000081386), ZNF506 (ENSG00000081665), ZNF268 (ENSG00000090612), MZF1 (ENSG00000099326), ZNF629 (ENSG00000102870), ZNF175 (ENSG00000105497), ZNF85 (ENSG00000105750), ZFP30 (ENSG00000120784), ZNF45 (ENSG00000124459), ZNF391 (ENSG00000124613), ZNF436 (ENSG00000125945), ZNF484 (ENSG00000127081), ZNF835 (ENSG00000127903), ZNF780B (ENSG00000128000), ZSCAN10 (ENSG00000130182), ZNF317 (ENSG00000130803), ZNF331 (ENSG00000130844), ZNF227 (ENSG00000131115), ZNF141 (ENSG00000131127), ZNF132 (ENSG00000131849), ZNF189 (ENSG00000136870), ZIM3 (ENSG00000141946), ZFP14 (ENSG00000142065), ZNF514 (ENSG00000144026), ZNF300 (ENSG00000145908), RBAK (ENSG00000146587), ZNF157 (ENSG00000147117), ZNF182 (ENSG00000147118), ZNF41 (ENSG00000147124), ZNF7 (ENSG00000147789), ZNF117 (ENSG00000152926), ZNF221 (ENSG00000159905), ZNF235 (ENSG00000159917), ZNF714 (ENSG00000160352), ZNF577 (ENSG00000161551), ZNF12 (ENSG00000164631)

Protein

Protein identifiers

Zinc finger protein 432O94892 (reviewed: O94892)

All UniProt accessions (5): O94892, M0QZ71, M0R0E2, M0R0H8, M0R258

UniProt curated annotations — full annotation on UniProt →

Function. Homologous recombination repressor that functions as a poly(ADP-ribose) (PAR) reader regulating DNA damage response and PARP inhibition. Once recruited to DNA lesions via DNA-, in a PAR-dependent mechanism, stimulates PARP1 activity. Binds preferentially ssDNA and inhibits EXO1-mediated resection, probably through a PAR-independent DNA-binding mechanism.

Subunit / interactions. Interacts with PARP1 and several chromatin remodeling proteins; the interaction with PARP1 reshapes ZNF432 interacting proteins. Interacts with TRIM28; the interaction is independent of PARP1.

Subcellular location. Nucleus.

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

RefSeq proteins (3): NP_001309213, NP_001309214, NP_055465* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (26 total): zinc finger region 16, modified residue 6, sequence variant 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-O94892-F172.560.18

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 (6): 41, 139, 164, 246, 330, 414

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 71 (showing top): GOBP_DNA_DAMAGE_RESPONSE, CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_5, LIAO_METASTASIS, MODULE_397, CHEN_HOXA5_TARGETS_9HR_UP, GOCC_NUCLEOLUS, PHONG_TNF_RESPONSE_NOT_VIA_P38, ATF2_UP.V1_DN, OISHI_CHOLANGIOMA_STEM_CELL_LIKE_UP, STK33_SKM_UP, CIITA_TARGET_GENES, NFE2L1_TARGET_GENES, ZNF274_TARGET_GENES, ZNF350_TARGET_GENES, ZNF766_TARGET_GENES

GO Biological Process (2): regulation of DNA-templated transcription (GO:0006355), DNA damage response (GO:0006974)

GO Molecular Function (6): damaged DNA binding (GO:0003684), zinc ion binding (GO:0008270), protein-macromolecule adaptor activity (GO:0030674), DNA binding (GO:0003677), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (2): nucleus (GO:0005634), nucleoplasm (GO:0005654)

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
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
cellular response to stress1
DNA binding1
transition metal ion binding1
protein binding1
molecular adaptor activity1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1
nuclear lumen1
cellular anatomical structure1

Protein interactions and networks

STRING

662 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF432GRIP2Q9C0E4470
ZNF432IRAK2O43187408
ZNF432RHPN2Q8IUC4405
ZNF432PSMA2P25787380
ZNF432OR4C5Q8NGB2378
ZNF432ACAP1Q15027376
ZNF432LILRA4P59901369
ZNF432KCTD1Q719H9366
ZNF432PAQR3Q6TCH7355
ZNF432APMAPQ9HDC9325
ZNF432KIAA1671Q9BY89316
ZNF432IL36AQ9UHA7311
ZNF432C2CD4CQ8TF44305
ZNF432LRRC4CQ9HCJ2290
ZNF432PRKAR1BP31321280

IntAct

11 interactions, top by confidence:

ABTypeScore
ZNF432DCDC2psi-mi:“MI:0915”(physical association)0.560
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
SLC9A8ZNF432psi-mi:“MI:0914”(association)0.530
ZNF432PGRMC1psi-mi:“MI:0915”(physical association)0.400
TRIM28ZNF320psi-mi:“MI:0914”(association)0.350
ZNF248SYN3psi-mi:“MI:0914”(association)0.350
SLC9A8AP1G1psi-mi:“MI:0914”(association)0.350
NDEL1ZNF432psi-mi:“MI:0915”(physical association)0.000
ZNF432DCDC2psi-mi:“MI:0915”(physical association)0.000

BioGRID (13): ZNF432 (Affinity Capture-MS), ZNF432 (Two-hybrid), ZNF432 (Proximity Label-MS), ZNF432 (Affinity Capture-MS), ZNF432 (Affinity Capture-MS), ZNF432 (Affinity Capture-MS), ZNF432 (Affinity Capture-MS), ZNF432 (Affinity Capture-MS), HSPE1 (Cross-Linking-MS (XL-MS)), ZNF432 (Affinity Capture-MS), ZNF432 (Affinity Capture-RNA), ZNF432 (Proximity Label-MS), ZNF432 (Proximity Label-MS)

ESM2 similar proteins: A2VDP4, A6NHJ4, O94892, P0CJ79, P17014, P17021, P17025, P17032, P17035, P18733, P51508, P51814, Q06730, Q06732, Q09FC8, Q0VGE8, Q14586, Q32M78, Q3MIS6, Q5JVG2, Q5R4K8, Q5R9S5, Q5RBQ3, Q5RCJ2, Q5RER9, Q5TYW1, Q5VIY5, Q6P560, Q6PDB4, Q6ZMW2, Q6ZN06, Q6ZNA1, Q76KX8, Q7L2R6, Q86Y25, Q8N184, Q8N823, Q8N883, Q8N8J6, Q8NEP9

Diamond homologs: A0JPL0, A2VDP4, A6QLU5, A6QPT6, A8MQ14, A8MUZ8, A8MWA4, B1APH4, B2RXC5, E9PYI1, E9Q8G5, O75290, O94892, P08042, P0CH99, P0CI00, P17014, P17025, P17030, P17031, P17032, P17098, P21506, P51508, P51523, P51786, P51814, P52736, P52738, Q02525, Q03923, Q03936, Q06730, Q06732, Q0VCB0, Q13401, Q14587, Q16587, Q2M218, Q2M3X9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance97
Likely benign6
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

1213 predictions. Top by Δscore:

VariantEffectΔscore
19:52035441:C:CCacceptor_gain1.0000
19:52040483:CATA:Cdonor_loss1.0000
19:52040579:ATAAC:Aacceptor_gain1.0000
19:52040580:TAAC:Tacceptor_gain1.0000
19:52040581:AAC:Aacceptor_gain1.0000
19:52040582:AC:Aacceptor_gain1.0000
19:52040583:CC:Cacceptor_gain1.0000
19:52040583:CCTGT:Cacceptor_loss1.0000
19:52040584:C:CCacceptor_gain1.0000
19:52040588:T:Cacceptor_gain1.0000
19:52040588:T:TCacceptor_gain1.0000
19:52040592:G:Tacceptor_gain1.0000
19:52041474:CCTCA:Cdonor_loss1.0000
19:52041475:CTCA:Cdonor_loss1.0000
19:52041476:TCACC:Tdonor_loss1.0000
19:52041477:CACCC:Cdonor_loss1.0000
19:52041478:A:ACdonor_gain1.0000
19:52041478:A:AGdonor_loss1.0000
19:52041478:AC:Adonor_gain1.0000
19:52041479:C:CCdonor_gain1.0000
19:52041479:C:CGdonor_loss1.0000
19:52041479:CC:Cdonor_gain1.0000
19:52041602:AATTC:Aacceptor_gain1.0000
19:52041603:ATTC:Aacceptor_gain1.0000
19:52041604:TTC:Tacceptor_gain1.0000
19:52041605:TC:Tacceptor_gain1.0000
19:52041606:CC:Cacceptor_gain1.0000
19:52041607:C:CCacceptor_gain1.0000
19:52076951:T:Adonor_gain1.0000
19:52076953:CTCA:Cdonor_loss1.0000

AlphaMissense

4378 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:52034333:C:GR449P0.998
19:52034669:C:GR337P0.998
19:52034701:G:CF326L0.998
19:52034701:G:TF326L0.998
19:52034703:A:GF326L0.998
19:52034081:C:GR533P0.997
19:52034113:A:CF522L0.997
19:52034113:A:TF522L0.997
19:52034115:A:GF522L0.997
19:52034197:G:CF494L0.997
19:52034197:G:TF494L0.997
19:52034199:A:GF494L0.997
19:52034365:A:CF438L0.997
19:52034365:A:TF438L0.997
19:52034367:A:GF438L0.997
19:52034449:A:CF410L0.997
19:52034449:A:TF410L0.997
19:52034451:A:GF410L0.997
19:52034785:G:CF298L0.997
19:52034785:G:TF298L0.997
19:52034787:A:GF298L0.997
19:52034165:C:GR505P0.996
19:52034249:C:GR477P0.996
19:52034281:G:CF466L0.996
19:52034281:G:TF466L0.996
19:52034283:A:GF466L0.996
19:52034533:G:CF382L0.996
19:52034533:G:TF382L0.996
19:52034535:A:GF382L0.996
19:52034672:T:GQ336P0.996

dbSNP variants (sampled 300 via entrez): RS1000031777 (19:52049378 T>C), RS1000040430 (19:52042653 T>A), RS1000083441 (19:52049191 G>T), RS1000140259 (19:52039571 C>T), RS1000325427 (19:52043991 C>A,G,T), RS1000380485 (19:52031251 C>T), RS1001114381 (19:52032441 T>TG), RS1001589927 (19:52045480 C>T), RS1001695135 (19:52050421 G>C), RS1001773783 (19:52045924 C>T), RS1001829200 (19:52041230 A>G), RS1001864533 (19:52040535 TCTC>T), RS1002328473 (19:52046765 A>G), RS1002335983 (19:52047546 C>A,T), RS1002487654 (19:52040836 G>A)

Disease associations

OMIM: gene MIM:620554 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

2 associations (top):

StudyTraitp-value
GCST002291_2Bronchodilator response in asthma (inhaled corticosteroid treatment interaction)2.000000e-09
GCST007277_24Tourette syndrome9.000000e-07

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

PharmGKB variants

1 variants.

VariantGenesLevelScore#Clin annotsDrugs
rs3752120ZNF4320.000

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
Valproic Aciddecreases expression3
arseniteaffects binding, decreases reaction, increases methylation2
Air Pollutantsdecreases expression, affects expression, increases abundance2
Particulate Matterdecreases expression, increases abundance2
triphenyl phosphateaffects expression1
propionaldehydeincreases expression1
sodium arseniteincreases expression1
di-n-butylphosphoric acidaffects expression1
pentabromodiphenyl etherincreases expression1
abrineincreases expression1
2,2’,4,4’-tetrabromodiphenyl etherincreases expression1
Grape Seed Proanthocyanidinsaffects cotreatment, decreases expression1
jinfukangaffects cotreatment, decreases expression1
theaflavin-3,3’-digallateaffects expression1
Resveratrolaffects cotreatment, increases expression1
Acetaminophenincreases expression1
Vehicle Emissionsdecreases expression, increases abundance1
Benzo(a)pyrenedecreases methylation1
Catechinaffects cotreatment, decreases expression1
Cisplatinaffects cotreatment, decreases expression1
Dimethyl Sulfoxideincreases expression1
Doxorubicindecreases expression1
Ethyl Methanesulfonateincreases expression1
Methyl Methanesulfonateincreases expression1
Ozoneaffects expression, increases abundance1
Plant Extractsaffects cotreatment, increases expression1
Plant Oilsincreases expression1
Tobacco Smoke Pollutionincreases expression1
Tretinoinincreases expression1
Aflatoxin B1increases methylation1

Cellosaurus cell lines

2 cell lines: 2 cancer cell line

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

CellosaurusNameCategorySex
CVCL_E0TCUbigene HeLa ZNF432 KOCancer cell lineFemale
CVCL_E1E0Ubigene U2OS ZNF432 KOCancer 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.