ZNF728

gene
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Summary

ZNF728 (zinc finger protein 728, HGNC:32463) is a protein-coding gene on chromosome 19p12, encoding Zinc finger protein 728 (P0DKX0).

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 388523 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 6 total
  • MANE Select transcript: NM_001267716

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:32463
Approved symbolZNF728
Namezinc finger protein 728
Location19p12
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000269067
Ensembl biotypeprotein_coding
Entrez388523

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000594710, ENST00000599851

RefSeq mRNA: 1 — MANE Select: NM_001267716 NM_001267716

CCDS: CCDS59370

Canonical transcript exons

ENST00000594710 — 4 exons

ExonStartEnd
ENSE000029858982298730822987403
ENSE000030870982297488322977110
ENSE000030942292300302823003176
ENSE000031803072298832522988451

Expression profiles

Bgee: expression breadth ubiquitous, 117 present calls, max score 82.44.

FANTOM5 (CAGE): breadth broad, TPM avg 0.7062 / max 86.9228, expressed in 186 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1802600.6532182
1802590.052925

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.44gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.34gold quality
testisUBERON:000047371.19gold quality
right testisUBERON:000453470.51gold quality
corpus callosumUBERON:000233670.01gold quality
left testisUBERON:000453369.71gold quality
smooth muscle tissueUBERON:000113564.68gold quality
heart left ventricleUBERON:000208462.66gold quality
heartUBERON:000094862.02gold quality
right atrium auricular regionUBERON:000663161.37gold quality
islet of LangerhansUBERON:000000659.43gold quality
apex of heartUBERON:000209858.23gold quality
fallopian tubeUBERON:000388958.09gold quality
descending thoracic aortaUBERON:000234557.98gold quality
lower esophagus muscularis layerUBERON:003583357.87gold quality
lower esophagusUBERON:001347357.82gold quality
calcaneal tendonUBERON:000370157.28gold quality
right coronary arteryUBERON:000162557.19gold quality
ovaryUBERON:000099256.94gold quality
left ovaryUBERON:000211956.84gold quality
thoracic aortaUBERON:000151556.56gold quality
esophagogastric junction muscularis propriaUBERON:003584156.48gold quality
ascending aortaUBERON:000149656.40gold quality
left coronary arteryUBERON:000162656.27gold quality
urinary bladderUBERON:000125556.26gold quality
myometriumUBERON:000129656.16gold quality
gall bladderUBERON:000211055.26gold quality
left uterine tubeUBERON:000130355.10gold quality
body of uterusUBERON:000985354.36gold quality
caudate nucleusUBERON:000187354.19gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no2.27

Regulation

Is transcription factor: yes

JASPAR motifs

MotifNameFamily
MA2589.1ZNF728More than 3 adjacent zinc fingers

JASPAR matrix evidence (PMIDs): PMID:39605368

miRNA regulators (miRDB)

56 targeting ZNF728, 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-3925-3P100.0069.951237
HSA-MIR-3064-3P100.0070.091254
HSA-MIR-4776-3P100.0068.731340
HSA-MIR-6833-3P100.0070.633197
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-188-3P100.0068.761240
HSA-MIR-1212199.9966.64255
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-1229-3P99.9766.49906
HSA-MIR-548AN99.9770.912817
HSA-MIR-365899.9673.874379
HSA-MIR-23A-3P99.9574.243163
HSA-MIR-23B-3P99.9574.243163
HSA-MIR-23C99.9573.923192
HSA-MIR-6809-3P99.9171.453814
HSA-MIR-200A-5P99.7669.10949
HSA-MIR-200B-5P99.7669.05948
HSA-MIR-488-3P99.6168.791731
HSA-MIR-32599.5866.55358
HSA-MIR-1212299.5669.331672
HSA-MIR-642A-5P99.5165.101152
HSA-MIR-486-5P99.5170.39707
HSA-MIR-1224-5P99.4865.59803
HSA-MIR-766-3P99.4765.241811
HSA-MIR-21-5P99.4670.541035
HSA-MIR-391599.4568.491905
HSA-MIR-4667-3P99.2665.451608
HSA-MIR-590-5P99.2570.76930
HSA-MIR-806599.1970.381289

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 728P0DKX0 (reviewed: P0DKX0)

All UniProt accessions (2): P0DKX0, M0QZ07

RefSeq proteins (1): NP_001254645* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050329GLI_C2H2-zinc-fingerFamily

Pfam: PF00096, PF01352, PF13465, PF13912

UniProt features (16 total): zinc finger region 14, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0DKX0-F169.180.07

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 32 (showing top): chr19p12, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOBP_NEGATIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II, GOBP_NEGATIVE_REGULATION_OF_NUCLEOBASE_CONTAINING_COMPOUND_METABOLIC_PROCESS, GOBP_POSITIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, TRIP13_TARGET_GENES, MIR6833_3P, MIR6873_3P, MIR4768_5P, MIR892C_5P, MIR3925_3P, MIR3064_3P, MIR4511, MIR4776_3P

GO Biological Process (4): negative regulation of transcription by RNA polymerase II (GO:0000122), regulation of transcription by RNA polymerase II (GO:0006357), positive regulation of transcription by RNA polymerase II (GO:0045944), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (5): 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), transcription cis-regulatory region binding (GO:0000976), metal ion binding (GO:0046872)

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

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of transcription by RNA polymerase II3
transcription by RNA polymerase II3
RNA polymerase II transcription regulatory region sequence-specific DNA binding2
negative regulation of DNA-templated transcription1
regulation of DNA-templated transcription1
positive 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
transcription regulatory region nucleic acid binding1
sequence-specific double-stranded DNA binding1
cation binding1
intracellular membrane-bounded organelle1
nucleus1
intracellular organelle lumen1

Protein interactions and networks

STRING

198 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF728CFAP96A7E2U8503
ZNF728ESRP1Q6NXG1454
ZNF728NFYBP25208447
ZNF728TTC29Q8NA56393
ZNF728DNAH11Q96DT5378
ZNF728DMRTC2Q8IXT2359
ZNF728ZGLP1P0C6A0358
ZNF728ICA1LQ8NDH6353
ZNF728CYP20A1Q6UW02350
ZNF728GK5Q6ZS86328
ZNF728ANKRD28O15084303
ZNF728RP1L1Q8IWN7267
ZNF728LOXHD1Q8IVV2261
ZNF728CWC22Q9HCG8257
ZNF728SIX2Q9NPC8254

IntAct

0 interactions, top by confidence:

BioGRID (3): ZNF728 (Positive Genetic), ZNF728 (Affinity Capture-MS), ZNF728 (Proximity Label-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

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance1
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

719 predictions. Top by Δscore:

VariantEffectΔscore
19:22977111:C:CCacceptor_gain1.0000
19:22988364:T:Adonor_gain1.0000
19:22988447:GATCC:Gacceptor_gain1.0000
19:22988449:TCC:Tacceptor_gain1.0000
19:22988450:CC:Cacceptor_gain1.0000
19:22988450:CCC:Cacceptor_gain1.0000
19:22988451:CC:Cacceptor_gain1.0000
19:22988451:CCTG:Cacceptor_loss1.0000
19:22988452:C:CAacceptor_loss1.0000
19:22988452:C:CCacceptor_gain1.0000
19:22988453:T:Aacceptor_loss1.0000
19:23003024:TCAC:Tdonor_loss1.0000
19:23003025:CA:Cdonor_loss1.0000
19:23003026:A:Cdonor_loss1.0000
19:22977106:TATAA:Tacceptor_gain0.9900
19:22977107:ATAA:Aacceptor_gain0.9900
19:22977108:TAA:Tacceptor_gain0.9900
19:22977572:G:Cdonor_gain0.9900
19:22988319:TCTCA:Tdonor_loss0.9900
19:22988320:CTCA:Cdonor_loss0.9900
19:22988321:TCA:Tdonor_loss0.9900
19:22988322:C:CGdonor_loss0.9900
19:22988323:A:ACdonor_gain0.9900
19:22988323:A:Cdonor_loss0.9900
19:22988323:AC:Adonor_gain0.9900
19:22988324:C:CCdonor_gain0.9900
19:22988324:CC:Cdonor_gain0.9900
19:22988448:ATCC:Aacceptor_gain0.9900
19:23003026:A:ACdonor_gain0.9900
19:23003026:AC:Adonor_gain0.9900

AlphaMissense

4148 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:22975786:G:CF517L0.987
19:22975786:G:TF517L0.987
19:22975788:A:GF517L0.987
19:22975618:A:CF573L0.985
19:22975618:A:TF573L0.985
19:22975620:A:GF573L0.985
19:22976458:A:CF293L0.983
19:22976458:A:TF293L0.983
19:22976460:A:GF293L0.983
19:22976206:G:CF377L0.982
19:22976206:G:TF377L0.982
19:22976208:A:GF377L0.982
19:22976374:G:CF321L0.978
19:22976374:G:TF321L0.978
19:22976376:A:GF321L0.978
19:22975702:G:CF545L0.977
19:22975702:G:TF545L0.977
19:22975704:A:GF545L0.977
19:22976542:G:CF265L0.970
19:22976542:G:TF265L0.970
19:22976544:A:GF265L0.970
19:22975870:A:CF489L0.968
19:22975870:A:TF489L0.968
19:22975872:A:GF489L0.968
19:22976038:A:CF433L0.966
19:22976038:A:TF433L0.966
19:22976040:A:GF433L0.966
19:22976290:A:CF349L0.965
19:22976290:A:TF349L0.965
19:22976292:A:GF349L0.965

dbSNP variants (sampled 300 via entrez): RS1000010482 (19:22998216 G>C), RS1000064182 (19:22997998 C>T), RS1000334976 (19:23003330 A>G,T), RS1001040311 (19:22978911 G>A), RS1001052970 (19:22979275 T>A), RS1001087815 (19:22985913 C>A), RS1001369740 (19:22991514 G>T), RS1001426119 (19:22984277 G>A), RS1001450099 (19:22978567 G>C), RS1001732689 (19:22996380 C>A,T), RS1002032102 (19:22995057 T>C,G), RS1002359542 (19:23000963 CAT>C), RS1002433197 (19:22988778 G>A,T), RS1002682548 (19:23005028 G>A), RS1002870736 (19:22982471 A>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

2 associations (top):

StudyTraitp-value
GCST002104_26Bronchopulmonary dysplasia4.000000e-06
GCST004713_9Testicular germ cell tumor5.000000e-14

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

8 total (human), top 8 by PubMed support.

ChemicalActions (top 5)PubMed papers
Cadmium Chloridedecreases expression, increases abundance, increases expression2
FR900359increases phosphorylation1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
manganese chlorideaffects cotreatment, increases abundance, increases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Cadmiumincreases abundance, increases expression1
Manganeseincreases expression, affects cotreatment, increases abundance1
Tetrachlorodibenzodioxinaffects expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.