ZNF732
gene geneOn 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
| Field | Value |
|---|---|
| HGNC ID | HGNC:37138 |
| Approved symbol | ZNF732 |
| Name | zinc finger protein 732 |
| Location | 4p16.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | FLJ59067 |
| Ensembl gene | ENSG00000186777 |
| Ensembl biotype | protein_coding |
| Entrez | 654254 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00001608370 | 305308 | 305474 |
| ENSE00001643036 | 270675 | 272630 |
| ENSE00001664041 | 295438 | 295533 |
| ENSE00001674937 | 296029 | 296155 |
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 ID | TPM avg | Samples expressed |
|---|---|---|
| 50983 | 1.5965 | 461 |
Top tissues by expression
130 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 80.99 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 77.76 | gold quality |
| ventricular zone | UBERON:0003053 | 69.04 | gold quality |
| tonsil | UBERON:0002372 | 61.47 | gold quality |
| ganglionic eminence | UBERON:0004023 | 61.13 | gold quality |
| cerebellar cortex | UBERON:0002129 | 60.66 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 60.62 | gold quality |
| cerebellum | UBERON:0002037 | 60.48 | gold quality |
| endometrium | UBERON:0001295 | 59.71 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 59.69 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 59.27 | gold quality |
| primary visual cortex | UBERON:0002436 | 56.97 | gold quality |
| colonic epithelium | UBERON:0000397 | 56.93 | silver quality |
| calcaneal tendon | UBERON:0003701 | 56.51 | gold quality |
| cortical plate | UBERON:0005343 | 55.87 | gold quality |
| placenta | UBERON:0001987 | 55.85 | gold quality |
| left ovary | UBERON:0002119 | 55.01 | gold quality |
| ovary | UBERON:0000992 | 54.50 | gold quality |
| body of uterus | UBERON:0009853 | 54.18 | gold quality |
| lymph node | UBERON:0000029 | 53.90 | gold quality |
| islet of Langerhans | UBERON:0000006 | 53.88 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 53.51 | gold quality |
| nucleus accumbens | UBERON:0001882 | 53.46 | gold quality |
| myometrium | UBERON:0001296 | 53.45 | gold quality |
| urinary bladder | UBERON:0001255 | 53.32 | gold quality |
| uterine cervix | UBERON:0000002 | 53.15 | gold quality |
| adrenal tissue | UBERON:0018303 | 53.12 | gold quality |
| pituitary gland | UBERON:0000007 | 52.78 | gold quality |
| adenohypophysis | UBERON:0002196 | 52.27 | gold quality |
| brain | UBERON:0000955 | 51.84 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.06 |
Regulation
Is transcription factor: yes
JASPAR motifs
| Motif | Name | Family |
|---|---|---|
| MA2528.1 | ZNF732 | More 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):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-3064-3P | 100.00 | 70.09 | 1254 |
| HSA-MIR-188-3P | 100.00 | 68.76 | 1240 |
| HSA-MIR-3925-3P | 100.00 | 69.95 | 1237 |
| HSA-MIR-4776-3P | 100.00 | 68.73 | 1340 |
| HSA-MIR-12121 | 99.99 | 66.64 | 255 |
| HSA-MIR-4715-3P | 99.98 | 66.03 | 670 |
| HSA-MIR-23A-3P | 99.95 | 74.24 | 3163 |
| HSA-MIR-23B-3P | 99.95 | 74.24 | 3163 |
| HSA-MIR-23C | 99.95 | 73.92 | 3192 |
| HSA-MIR-4713-5P | 99.78 | 67.80 | 1794 |
| HSA-MIR-3156-3P | 99.76 | 66.72 | 939 |
| HSA-MIR-2116-3P | 99.74 | 64.32 | 889 |
| HSA-MIR-10393-5P | 99.65 | 68.01 | 1368 |
| HSA-MIR-1251-3P | 99.64 | 67.21 | 1408 |
| HSA-MIR-6126 | 99.62 | 68.09 | 996 |
| HSA-MIR-1260A | 99.61 | 66.67 | 1098 |
| HSA-MIR-1260B | 99.61 | 66.67 | 1098 |
| HSA-MIR-136-5P | 99.50 | 67.26 | 1153 |
| HSA-MIR-6833-5P | 99.50 | 68.93 | 1161 |
| HSA-MIR-766-3P | 99.47 | 65.24 | 1811 |
| HSA-MIR-6853-3P | 99.36 | 70.79 | 1558 |
| HSA-MIR-296-3P | 99.21 | 66.56 | 474 |
| HSA-MIR-4464 | 98.95 | 67.73 | 820 |
| HSA-MIR-4748 | 98.95 | 67.53 | 810 |
| HSA-MIR-412-3P | 98.86 | 66.89 | 712 |
| HSA-MIR-6754-3P | 98.84 | 66.60 | 889 |
| HSA-MIR-4751 | 98.80 | 64.95 | 525 |
| HSA-MIR-11399 | 98.71 | 65.69 | 869 |
| HSA-MIR-4752 | 98.71 | 68.04 | 833 |
| HSA-MIR-6837-3P | 98.42 | 66.71 | 1149 |
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 732 — B4DXR9 (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)
| ID | Name | Type |
|---|---|---|
| IPR001909 | KRAB | Domain |
| IPR013087 | Znf_C2H2_type | Domain |
| IPR036051 | KRAB_dom_sf | Homologous_superfamily |
| IPR036236 | Znf_C2H2_sf | Homologous_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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-B4DXR9-F1 | 69.25 | 0.13 |
Function
Pathways and Gene Ontology
Reactome pathways
1 pathways
| ID | Pathway |
|---|---|
| R-HSA-212436 | Generic 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:
| Category | Pathways |
|---|---|
| RNA Polymerase II Transcription | 1 |
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| regulation of transcription by RNA polymerase II | 2 |
| RNA polymerase II transcription regulatory region sequence-specific DNA binding | 2 |
| transcription by RNA polymerase II | 1 |
| negative regulation of DNA-templated transcription | 1 |
| DNA-templated transcription | 1 |
| regulation of gene expression | 1 |
| regulation of RNA biosynthetic process | 1 |
| cis-regulatory region sequence-specific DNA binding | 1 |
| chromatin | 1 |
| DNA-binding transcription factor activity | 1 |
| transition metal ion binding | 1 |
| nucleic acid binding | 1 |
| DNA binding | 1 |
| cation binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
184 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| ZNF732 | ANKS4B | Q8N8V4 | 505 |
| ZNF732 | TRAPPC12 | Q8WVT3 | 447 |
| ZNF732 | SNTG2 | Q9NY99 | 407 |
| ZNF732 | MAGEB2 | O15479 | 402 |
| ZNF732 | POLN | Q7Z5Q5 | 400 |
| ZNF732 | SUSD1 | Q6UWL2 | 393 |
| ZNF732 | HDHD2 | Q9H0R4 | 371 |
| ZNF732 | CCDC7 | Q96M83 | 371 |
| ZNF732 | TMEM35B | Q8NCS4 | 348 |
| ZNF732 | PHYHD1 | Q5SRE7 | 334 |
| ZNF732 | FBXL13 | Q8NEE6 | 320 |
| ZNF732 | MRTFB | Q9ULH7 | 318 |
| ZNF732 | CCDC8 | Q9H0W5 | 273 |
| ZNF732 | AKNA | Q7Z591 | 267 |
| ZNF732 | ZCCHC8 | Q6NZY4 | 264 |
IntAct
8 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| TRIM28 | ZNF320 | psi-mi:“MI:0914”(association) | 0.530 |
| ECE1 | ZNF732 | psi-mi:“MI:0915”(physical association) | 0.370 |
| TRIM28 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| PURG | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| MCEE | ZNF732 | psi-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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 96 |
| Likely benign | 11 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
687 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 4:296012:A:AC | donor_gain | 1.0000 |
| 4:296013:C:CC | donor_gain | 1.0000 |
| 4:272626:CACAG:C | acceptor_gain | 0.9900 |
| 4:272628:CAG:C | acceptor_gain | 0.9900 |
| 4:295432:ACCT:A | donor_loss | 0.9900 |
| 4:295433:CCTA:C | donor_loss | 0.9900 |
| 4:295434:CT:C | donor_loss | 0.9900 |
| 4:295435:TACCT:T | donor_loss | 0.9900 |
| 4:295436:ACCTG:A | donor_loss | 0.9900 |
| 4:295437:CC:C | donor_loss | 0.9900 |
| 4:295532:ACCTG:A | acceptor_loss | 0.9900 |
| 4:295533:CCTG:C | acceptor_loss | 0.9900 |
| 4:296023:CCTCA:C | donor_loss | 0.9900 |
| 4:296024:CTCAC:C | donor_loss | 0.9900 |
| 4:296027:A:AG | donor_loss | 0.9900 |
| 4:296028:CCCAG:C | donor_loss | 0.9900 |
| 4:272631:C:CC | acceptor_gain | 0.9800 |
| 4:295430:TCAC:T | donor_loss | 0.9800 |
| 4:295431:CACC:C | donor_loss | 0.9800 |
| 4:295536:G:C | acceptor_loss | 0.9800 |
| 4:295986:C:CA | donor_gain | 0.9800 |
| 4:296021:AT:A | donor_gain | 0.9800 |
| 4:296021:ATCCT:A | donor_loss | 0.9800 |
| 4:295438:C:A | donor_loss | 0.9700 |
| 4:295531:CAC:C | acceptor_gain | 0.9700 |
| 4:296027:AC:A | donor_gain | 0.9700 |
| 4:296028:CC:C | donor_gain | 0.9700 |
| 4:295429:GTCAC:G | donor_loss | 0.9600 |
| 4:296044:T:TA | donor_gain | 0.9600 |
| 4:296154:TCC:T | acceptor_loss | 0.9600 |
AlphaMissense
3893 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 4:271828:A:C | F343L | 0.996 |
| 4:271828:A:T | F343L | 0.996 |
| 4:271830:A:G | F343L | 0.996 |
| 4:271744:A:C | F371L | 0.992 |
| 4:271744:A:T | F371L | 0.992 |
| 4:271746:A:G | F371L | 0.992 |
| 4:271660:A:C | F399L | 0.988 |
| 4:271660:A:T | F399L | 0.988 |
| 4:271662:A:G | F399L | 0.988 |
| 4:271492:A:C | F455L | 0.987 |
| 4:271492:A:T | F455L | 0.987 |
| 4:271494:A:G | F455L | 0.987 |
| 4:271324:A:C | F511L | 0.979 |
| 4:271324:A:T | F511L | 0.979 |
| 4:271326:A:G | F511L | 0.979 |
| 4:271727:A:G | L377P | 0.978 |
| 4:271829:A:G | F343S | 0.974 |
| 4:271576:A:C | F427L | 0.973 |
| 4:271576:A:T | F427L | 0.973 |
| 4:271578:A:G | F427L | 0.973 |
| 4:296120:G:C | F13L | 0.973 |
| 4:296120:G:T | F13L | 0.973 |
| 4:296122:A:G | F13L | 0.973 |
| 4:271408:A:C | F483L | 0.972 |
| 4:271408:A:T | F483L | 0.972 |
| 4:271410:A:G | F483L | 0.972 |
| 4:271705:A:C | H384Q | 0.965 |
| 4:271705:A:T | H384Q | 0.965 |
| 4:271739:T:G | Q373P | 0.964 |
| 4:271912:A:C | F315L | 0.964 |
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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| bisphenol A | decreases methylation | 1 |
| sodium arsenite | decreases expression | 1 |
| potassium chromate(VI) | increases expression | 1 |
| Benzo(a)pyrene | affects methylation | 1 |
| Cadmium Chloride | decreases expression | 1 |
| p-Chloromercuribenzoic Acid | increases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.