ZNF732

gene
On this page

Also known as FLJ59067

Summary

ZNF732 (zinc finger protein 732, HGNC:37138) is a protein-coding gene on chromosome 4p16.3, encoding Zinc finger protein 732 (B4DXR9). May be involved in transcriptional regulation.

This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and sixteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation.

Source: NCBI Gene 654254 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 109 total
  • MANE Select transcript: NM_001137608

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:37138
Approved symbolZNF732
Namezinc finger protein 732
Location4p16.3
Locus typegene with protein product
StatusApproved
AliasesFLJ59067
Ensembl geneENSG00000186777
Ensembl biotypeprotein_coding
Entrez654254

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000419098

RefSeq mRNA: 1 — MANE Select: NM_001137608 NM_001137608

CCDS: CCDS46990

Canonical transcript exons

ENST00000419098 — 4 exons

ExonStartEnd
ENSE00001608370305308305474
ENSE00001643036270675272630
ENSE00001664041295438295533
ENSE00001674937296029296155

Expression profiles

Bgee: expression breadth ubiquitous, 120 present calls, max score 80.99.

FANTOM5 (CAGE): breadth broad, TPM avg 1.5965 / max 62.0633, expressed in 461 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
509831.5965461

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.99gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.76gold quality
ventricular zoneUBERON:000305369.04gold quality
tonsilUBERON:000237261.47gold quality
ganglionic eminenceUBERON:000402361.13gold quality
cerebellar cortexUBERON:000212960.66gold quality
cerebellar hemisphereUBERON:000224560.62gold quality
cerebellumUBERON:000203760.48gold quality
endometriumUBERON:000129559.71gold quality
right hemisphere of cerebellumUBERON:001489059.69gold quality
lower esophagus mucosaUBERON:003583459.27gold quality
primary visual cortexUBERON:000243656.97gold quality
colonic epitheliumUBERON:000039756.93silver quality
calcaneal tendonUBERON:000370156.51gold quality
cortical plateUBERON:000534355.87gold quality
placentaUBERON:000198755.85gold quality
left ovaryUBERON:000211955.01gold quality
ovaryUBERON:000099254.50gold quality
body of uterusUBERON:000985354.18gold quality
lymph nodeUBERON:000002953.90gold quality
islet of LangerhansUBERON:000000653.88gold quality
superior frontal gyrusUBERON:000266153.51gold quality
nucleus accumbensUBERON:000188253.46gold quality
myometriumUBERON:000129653.45gold quality
urinary bladderUBERON:000125553.32gold quality
uterine cervixUBERON:000000253.15gold quality
adrenal tissueUBERON:001830353.12gold quality
pituitary glandUBERON:000000752.78gold quality
adenohypophysisUBERON:000219652.27gold quality
brainUBERON:000095551.84gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.06

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2528.1ZNF732More than 3 adjacent zinc fingers

JASPAR matrix evidence (PMIDs): PMID:39605530

miRNA regulators (miRDB)

46 targeting ZNF732, 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-3064-3P100.0070.091254
HSA-MIR-188-3P100.0068.761240
HSA-MIR-3925-3P100.0069.951237
HSA-MIR-4776-3P100.0068.731340
HSA-MIR-1212199.9966.64255
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-23A-3P99.9574.243163
HSA-MIR-23B-3P99.9574.243163
HSA-MIR-23C99.9573.923192
HSA-MIR-4713-5P99.7867.801794
HSA-MIR-3156-3P99.7666.72939
HSA-MIR-2116-3P99.7464.32889
HSA-MIR-10393-5P99.6568.011368
HSA-MIR-1251-3P99.6467.211408
HSA-MIR-612699.6268.09996
HSA-MIR-1260A99.6166.671098
HSA-MIR-1260B99.6166.671098
HSA-MIR-136-5P99.5067.261153
HSA-MIR-6833-5P99.5068.931161
HSA-MIR-766-3P99.4765.241811
HSA-MIR-6853-3P99.3670.791558
HSA-MIR-296-3P99.2166.56474
HSA-MIR-446498.9567.73820
HSA-MIR-474898.9567.53810
HSA-MIR-412-3P98.8666.89712
HSA-MIR-6754-3P98.8466.60889
HSA-MIR-475198.8064.95525
HSA-MIR-1139998.7165.69869
HSA-MIR-475298.7168.04833
HSA-MIR-6837-3P98.4266.711149

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 732B4DXR9 (reviewed: B4DXR9)

All UniProt accessions (1): B4DXR9

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_001131080* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352, PF13912

UniProt features (18 total): zinc finger region 16, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-B4DXR9-F169.250.13

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 37 (showing top): chr4p16, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOBP_NEGATIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II, GOBP_NEGATIVE_REGULATION_OF_NUCLEOBASE_CONTAINING_COMPOUND_METABOLIC_PROCESS, ZWANG_DOWN_BY_2ND_EGF_PULSE, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, HMGA1_TARGET_GENES, HSD17B8_TARGET_GENES, PRKDC_TARGET_GENES, MIR3925_3P, MIR3064_3P, MIR188_3P, MIR4776_3P, MIR766_3P, MIR1251_3P

GO Biological Process (2): negative regulation of transcription by RNA polymerase II (GO:0000122), 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), double-stranded DNA binding (GO:0003690), 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 transcription by RNA polymerase II2
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
transcription by RNA polymerase II1
negative regulation of DNA-templated transcription1
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
transition metal ion binding1
nucleic acid binding1
DNA binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

184 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF732ANKS4BQ8N8V4505
ZNF732TRAPPC12Q8WVT3447
ZNF732SNTG2Q9NY99407
ZNF732MAGEB2O15479402
ZNF732POLNQ7Z5Q5400
ZNF732SUSD1Q6UWL2393
ZNF732HDHD2Q9H0R4371
ZNF732CCDC7Q96M83371
ZNF732TMEM35BQ8NCS4348
ZNF732PHYHD1Q5SRE7334
ZNF732FBXL13Q8NEE6320
ZNF732MRTFBQ9ULH7318
ZNF732CCDC8Q9H0W5273
ZNF732AKNAQ7Z591267
ZNF732ZCCHC8Q6NZY4264

IntAct

8 interactions, top by confidence:

ABTypeScore
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ECE1ZNF732psi-mi:“MI:0915”(physical association)0.370
TRIM28ZNF320psi-mi:“MI:0914”(association)0.350
PURGZNF320psi-mi:“MI:0914”(association)0.350
MCEEZNF732psi-mi:“MI:0914”(association)0.350

BioGRID (4): ZNF732 (Affinity Capture-MS), ZNF732 (Affinity Capture-MS), ZNF732 (Affinity Capture-MS), ZNF732 (Affinity Capture-MS)

ESM2 similar proteins: A6NDX5, A6NK75, A6NNF4, A6NP11, B4DXR9, B7Z6K7, C9JN71, O43361, O75290, O75373, P0CJ79, P0DKX0, P17019, P17021, P17035, P17039, P35789, Q02386, Q03938, Q08AN1, Q13106, Q15928, Q3ZCX4, Q5R9F0, Q5SXM1, Q68EA5, Q6P9A1, Q6PDB4, Q6ZN06, Q6ZN08, Q6ZNG1, Q76KX8, Q86V71, Q86XN6, Q8IYB9, Q8N4W9, Q8NEP9, Q8TBZ8, Q8TC21, Q8TF32

Diamond homologs: A0A1W2PQL4, A6NK75, A6NN14, A6NNF4, A6NP11, A8MQ14, A8MTY0, A8MUV8, A8MXY4, B4DX44, B4DXR9, E9PYI1, O14628, O43345, O75290, O75346, O75373, O75437, O95780, P0CB33, P0DKX0, P0DPD5, P16373, P17019, P17038, P21506, P35789, P52736, P52738, P52744, Q03923, Q03924, Q03936, Q03938, Q05481, Q14586, Q14593, Q14929, Q15928, Q3KNS6

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 significance96
Likely benign11
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

687 predictions. Top by Δscore:

VariantEffectΔscore
4:296012:A:ACdonor_gain1.0000
4:296013:C:CCdonor_gain1.0000
4:272626:CACAG:Cacceptor_gain0.9900
4:272628:CAG:Cacceptor_gain0.9900
4:295432:ACCT:Adonor_loss0.9900
4:295433:CCTA:Cdonor_loss0.9900
4:295434:CT:Cdonor_loss0.9900
4:295435:TACCT:Tdonor_loss0.9900
4:295436:ACCTG:Adonor_loss0.9900
4:295437:CC:Cdonor_loss0.9900
4:295532:ACCTG:Aacceptor_loss0.9900
4:295533:CCTG:Cacceptor_loss0.9900
4:296023:CCTCA:Cdonor_loss0.9900
4:296024:CTCAC:Cdonor_loss0.9900
4:296027:A:AGdonor_loss0.9900
4:296028:CCCAG:Cdonor_loss0.9900
4:272631:C:CCacceptor_gain0.9800
4:295430:TCAC:Tdonor_loss0.9800
4:295431:CACC:Cdonor_loss0.9800
4:295536:G:Cacceptor_loss0.9800
4:295986:C:CAdonor_gain0.9800
4:296021:AT:Adonor_gain0.9800
4:296021:ATCCT:Adonor_loss0.9800
4:295438:C:Adonor_loss0.9700
4:295531:CAC:Cacceptor_gain0.9700
4:296027:AC:Adonor_gain0.9700
4:296028:CC:Cdonor_gain0.9700
4:295429:GTCAC:Gdonor_loss0.9600
4:296044:T:TAdonor_gain0.9600
4:296154:TCC:Tacceptor_loss0.9600

AlphaMissense

3893 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
4:271828:A:CF343L0.996
4:271828:A:TF343L0.996
4:271830:A:GF343L0.996
4:271744:A:CF371L0.992
4:271744:A:TF371L0.992
4:271746:A:GF371L0.992
4:271660:A:CF399L0.988
4:271660:A:TF399L0.988
4:271662:A:GF399L0.988
4:271492:A:CF455L0.987
4:271492:A:TF455L0.987
4:271494:A:GF455L0.987
4:271324:A:CF511L0.979
4:271324:A:TF511L0.979
4:271326:A:GF511L0.979
4:271727:A:GL377P0.978
4:271829:A:GF343S0.974
4:271576:A:CF427L0.973
4:271576:A:TF427L0.973
4:271578:A:GF427L0.973
4:296120:G:CF13L0.973
4:296120:G:TF13L0.973
4:296122:A:GF13L0.973
4:271408:A:CF483L0.972
4:271408:A:TF483L0.972
4:271410:A:GF483L0.972
4:271705:A:CH384Q0.965
4:271705:A:TH384Q0.965
4:271739:T:GQ373P0.964
4:271912:A:CF315L0.964

dbSNP variants (sampled 300 via entrez): RS1000035875 (4:287108 G>A,T), RS1000091614 (4:295889 C>T), RS1000189243 (4:289891 T>G), RS1000237308 (4:283861 A>G), RS10002733 (4:285607 A>C), RS10003142 (4:297970 C>A,G,T), RS10005733 (4:298212 C>A,G), RS1000613684 (4:277983 A>C), RS1000708285 (4:289601 G>A,T), RS1000720571 (4:271764 C>T), RS1000876669 (4:300961 A>T), RS1000985570 (4:294970 G>A,C), RS1001101484 (4:294605 G>C), RS1001270569 (4:302928 C>T), RS1001357061 (4:290243 C>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

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
bisphenol Adecreases methylation1
sodium arsenitedecreases expression1
potassium chromate(VI)increases expression1
Benzo(a)pyreneaffects methylation1
Cadmium Chloridedecreases expression1
p-Chloromercuribenzoic Acidincreases 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.