ZNF17

gene
On this page

Also known as HPF3KOX10KIAA1947FLJ40864FLJ46058FLJ46615

Summary

ZNF17 (zinc finger protein 17, HGNC:12958) is a protein-coding gene on chromosome 19q13.43, encoding Zinc finger protein 17 (P17021). 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 7565 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 96 total
  • MANE Select transcript: NM_001330617

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12958
Approved symbolZNF17
Namezinc finger protein 17
Location19q13.43
Locus typegene with protein product
StatusApproved
AliasesHPF3, KOX10, KIAA1947, FLJ40864, FLJ46058, FLJ46615
Ensembl geneENSG00000186272
Ensembl biotypeprotein_coding
OMIM619254
Entrez7565

Gene structure

Transcript identifiers

Ensembl transcripts: 10 — 6 protein_coding, 2 protein_coding_CDS_not_defined, 1 nonsense_mediated_decay, 1 retained_intron

ENST00000307658, ENST00000595162, ENST00000595206, ENST00000597350, ENST00000599867, ENST00000601808, ENST00000602050, ENST00000878542, ENST00000964805, ENST00000964806

RefSeq mRNA: 2 — MANE Select: NM_001330617 NM_001330617, NM_006959

CCDS: CCDS42636, CCDS82405

Canonical transcript exons

ENST00000307658 — 4 exons

ExonStartEnd
ENSE000011708225741963557421934
ENSE000031609595741116157411406
ENSE000036865705741359657413636
ENSE000037849195741791257418038

Expression profiles

Bgee: expression breadth ubiquitous, 136 present calls, max score 85.68.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.9803 / max 50.1750, expressed in 1507 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1777723.98031507

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.68gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047380.64gold quality
corpus callosumUBERON:000233680.34gold quality
ventricular zoneUBERON:000305379.26gold quality
cortical plateUBERON:000534379.26gold quality
calcaneal tendonUBERON:000370177.98gold quality
embryoUBERON:000092277.73gold quality
ganglionic eminenceUBERON:000402377.73gold quality
skeletal muscle tissueUBERON:000113477.12gold quality
tonsilUBERON:000237276.84gold quality
endometriumUBERON:000129576.00gold quality
muscle tissueUBERON:000238575.86gold quality
smooth muscle tissueUBERON:000113575.75gold quality
skeletal muscle organUBERON:001489275.48gold quality
muscle of legUBERON:000138375.42gold quality
gastrocnemiusUBERON:000138875.23gold quality
hindlimb stylopod muscleUBERON:000425275.18gold quality
apex of heartUBERON:000209875.12gold quality
islet of LangerhansUBERON:000000674.89gold quality
stromal cell of endometriumCL:000225574.67gold quality
urinary bladderUBERON:000125574.66gold quality
granulocyteCL:000009474.65gold quality
adrenal tissueUBERON:001830374.17gold quality
ovaryUBERON:000099274.09gold quality
lymph nodeUBERON:000002973.98gold quality
heart left ventricleUBERON:000208473.98gold quality
heartUBERON:000094873.91gold quality
superior frontal gyrusUBERON:000266173.83gold quality
descending thoracic aortaUBERON:000234573.81gold quality
left ovaryUBERON:000211973.65gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no3.58

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

27 targeting ZNF17, 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-32-5P99.9875.211964
HSA-MIR-363-3P99.9874.721821
HSA-MIR-367-3P99.9874.831819
HSA-MIR-92A-3P99.9875.211960
HSA-MIR-92B-3P99.9875.251955
HSA-MIR-485-3P99.9870.681585
HSA-MIR-539-3P99.9870.741616
HSA-MIR-302C-5P99.9772.563642
HSA-MIR-808299.9567.271170
HSA-MIR-10527-5P99.9172.283754
HSA-MIR-808799.9069.551351
HSA-MIR-450399.8571.451869
HSA-MIR-497-3P99.6169.711990
HSA-MIR-302B-5P99.5069.491857
HSA-MIR-302D-5P99.5069.341863
HSA-MIR-239299.4367.50708
HSA-MIR-6505-3P99.3467.391071
HSA-MIR-4777-5P99.3367.531148
HSA-MIR-329-5P99.2768.111597
HSA-MIR-664A-3P99.2271.082696
HSA-MIR-449B-3P99.2067.241047
HSA-MIR-125798.9768.021133
HSA-MIR-4742-3P98.7369.821803
HSA-MIR-431798.4967.09987
HSA-MIR-1912-5P97.9467.98832
HSA-MIR-63097.5066.38921
HSA-MIR-6831-3P97.4969.29505

Cross-species orthologs

0 orthologs

Paralogs (51): WIZ (ENSG00000011451), ZNF416 (ENSG00000083817), MYNN (ENSG00000085274), PRDM4 (ENSG00000110851), PRDM2 (ENSG00000116731), ZBTB17 (ENSG00000116809), ZNF644 (ENSG00000122482), GZF1 (ENSG00000125812), ZNF426 (ENSG00000130818), ZNF287 (ENSG00000141040), ZNF697 (ENSG00000143067), ZNF687 (ENSG00000143373), ZNF214 (ENSG00000149050), ZNF547 (ENSG00000152433), ZNF776 (ENSG00000152443), ZNF230 (ENSG00000159882), ZNF222 (ENSG00000159885), ZNF233 (ENSG00000159915), ZNF333 (ENSG00000160961), ZNF319 (ENSG00000166188), ZNF592 (ENSG00000166716), ZNF646 (ENSG00000167395), ZNF507 (ENSG00000168813), ZNF768 (ENSG00000169957), ZNF417 (ENSG00000173480), ZNF408 (ENSG00000175213), ZBTB41 (ENSG00000177888), ZNF223 (ENSG00000178386), ZNF852 (ENSG00000178917), ZNF784 (ENSG00000179922), ZNF572 (ENSG00000180938), ZNF707 (ENSG00000181135), ZNF746 (ENSG00000181220), ZNF467 (ENSG00000181444), ZNF530 (ENSG00000183647), ZNF527 (ENSG00000189164), ZKSCAN7 (ENSG00000196345), ZNF34 (ENSG00000196378), ZNF774 (ENSG00000196391), ZNF777 (ENSG00000196453)

Protein

Protein identifiers

Zinc finger protein 17P17021 (reviewed: P17021)

Alternative names: Zinc finger protein HPF3, Zinc finger protein KOX10

All UniProt accessions (3): P17021, M0QZR3, M0R2T2

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.

Isoforms (3)

UniProt IDNamesCanonical?
P17021-11yes
P17021-22
P17021-33

RefSeq proteins (2): NP_001317546, NP_008890 (=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (24 total): zinc finger region 16, sequence conflict 3, splice variant 2, chain 1, domain 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P17021-F173.170.16

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 37 (showing top): GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, ACACTGG_MIR199A_MIR199B, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, CEBPZ_TARGET_GENES, DLX4_TARGET_GENES, MIR10527_5P, MIR497_3P, MIR302B_5P, MIR302D_5P, MIR329_5P, MIR1257, MIR449B_3P, MIR630, MIR6831_3P, SMN1_SMN2_TARGET_GENES

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 (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
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

Protein interactions and networks

STRING

580 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF17OR10G2Q8NGC3447
ZNF17EFCAB8A8MWE9396
ZNF17C5orf15Q8NC54395
ZNF17ABHD1Q96SE0311
ZNF17MAMDC4Q6UXC1306
ZNF17SPAG17Q6Q759291
ZNF17CEP20Q96NB1290
ZNF17TMCC1O94876276
ZNF17SVILO95425272
ZNF17HOGA1Q86XE5261
ZNF17CORO2BQ9UQ03256
ZNF17UNC79Q9P2D8254
ZNF17GPR107Q5VW38252
ZNF17FAM111BQ6SJ93248
ZNF17SLC26A11Q86WA9247

IntAct

41 interactions, top by confidence:

ABTypeScore
ZNF17ZNF837psi-mi:“MI:0915”(physical association)0.560
ZNF17MTUS2psi-mi:“MI:0915”(physical association)0.560
GOLGA6L9ZNF17psi-mi:“MI:0915”(physical association)0.560
ZNF17PICK1psi-mi:“MI:0915”(physical association)0.560
ZNF17CEP70psi-mi:“MI:0915”(physical association)0.560
ZNF17OPTNpsi-mi:“MI:0915”(physical association)0.560
ZNF17ZRANB1psi-mi:“MI:0915”(physical association)0.560
ZNF17KRT40psi-mi:“MI:0915”(physical association)0.560
ZNF17SETpsi-mi:“MI:0915”(physical association)0.560
YJU2BZNF17psi-mi:“MI:0915”(physical association)0.560
ZNF17AIRIMpsi-mi:“MI:0915”(physical association)0.560
ZNF17ZNF438psi-mi:“MI:0915”(physical association)0.560
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
ZNF17TRIM24psi-mi:“MI:0914”(association)0.350
ZNF17NDEL1psi-mi:“MI:0915”(physical association)0.000
NDEL1ZNF17psi-mi:“MI:0915”(physical association)0.000
ZNF17ZNF837psi-mi:“MI:0915”(physical association)0.000
ZNF17MTUS2psi-mi:“MI:0915”(physical association)0.000
ZNF17GOLGA6L9psi-mi:“MI:0915”(physical association)0.000
ZNF17PICK1psi-mi:“MI:0915”(physical association)0.000
ZNF17CEP70psi-mi:“MI:0915”(physical association)0.000
ZNF17OPTNpsi-mi:“MI:0915”(physical association)0.000
ZNF17ZRANB1psi-mi:“MI:0915”(physical association)0.000
ZNF17KRT40psi-mi:“MI:0915”(physical association)0.000
AIRIMZNF17psi-mi:“MI:0915”(physical association)0.000
SETZNF17psi-mi:“MI:0915”(physical association)0.000
ZNF17YJU2Bpsi-mi:“MI:0915”(physical association)0.000

BioGRID (38): ZNF17 (Synthetic Growth Defect), ZNF17 (Affinity Capture-RNA), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), ZNF17 (Two-hybrid), GOLGA6L9 (Two-hybrid), KRT40 (Two-hybrid), DAP3 (Affinity Capture-MS)

ESM2 similar proteins: A0JNB1, A1YF12, A1YG88, A2T759, B2RUI1, O43296, O75123, P10072, P17020, P17021, P17097, P51814, P52740, P52741, Q07230, Q08ER8, Q13398, Q14590, Q32KN0, Q3KQV3, Q3MIS6, Q4V8A8, Q5CZA5, Q5RBQ3, Q5RBX0, Q5RCD9, Q5RCX4, Q6GQR8, Q6NX45, Q6P9A3, Q6PK81, Q7TSH9, Q7TSI0, Q7Z7L9, Q86UD4, Q8BFS8, Q8BLB0, Q8IVP9, Q8IZ26, Q8TAU3

Diamond homologs: A2RRD8, A6NFI3, A6NM28, A8MUZ8, A8MWA4, B2RUI1, B4DU55, E9Q8G5, O43296, O43361, O75467, O75820, P0CH99, P0CI00, P10078, P16373, P16374, P17021, P17023, P17032, P17097, P17098, P21506, P51786, P52740, Q06732, Q08ER8, Q13106, Q13360, Q13398, Q14592, Q147U1, Q32M78, Q3KQV3, Q3MIS6, Q3SY52, Q571J5, Q5CZA5, Q5HY98, Q5R7I8

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance84
Likely benign6
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

866 predictions. Top by Δscore:

VariantEffectΔscore
19:57418035:GTAG:Gdonor_gain1.0000
19:57411402:CTGAG:Cdonor_loss0.9900
19:57411403:TGAG:Tdonor_loss0.9900
19:57411405:AGGTG:Adonor_loss0.9900
19:57411407:G:GAdonor_loss0.9900
19:57411408:T:Gdonor_loss0.9900
19:57411006:C:Tdonor_gain0.9800
19:57411015:T:Gdonor_gain0.9800
19:57411015:T:TGdonor_gain0.9800
19:57411010:T:Gdonor_gain0.9700
19:57417911:GGATT:Gacceptor_gain0.9700
19:57418034:AGTAG:Adonor_loss0.9700
19:57418037:AG:Adonor_loss0.9700
19:57418038:GGTAA:Gdonor_loss0.9700
19:57418039:GTAA:Gdonor_loss0.9700
19:57418040:T:Gdonor_loss0.9700
19:57419634:GGTT:Gacceptor_gain0.9700
19:57411409:GGGT:Gdonor_loss0.9600
19:57411410:GGTG:Gdonor_loss0.9600
19:57417910:A:AGacceptor_gain0.9600
19:57417910:AG:Aacceptor_gain0.9600
19:57417911:G:GGacceptor_gain0.9600
19:57417911:GG:Gacceptor_gain0.9600
19:57419628:GTTTT:Gacceptor_loss0.9600
19:57419629:TTTTA:Tacceptor_loss0.9600
19:57419630:TTTA:Tacceptor_loss0.9600
19:57419631:TTA:Tacceptor_loss0.9600
19:57419631:TTAG:Tacceptor_loss0.9600
19:57419632:TA:Tacceptor_loss0.9600
19:57419633:A:ACacceptor_loss0.9600

AlphaMissense

4492 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:57421011:T:CF507L0.994
19:57421013:T:AF507L0.994
19:57421013:T:GF507L0.994
19:57421431:T:CF647L0.994
19:57421433:T:AF647L0.994
19:57421433:T:GF647L0.994
19:57420423:T:CF311L0.993
19:57420425:C:AF311L0.993
19:57420425:C:GF311L0.993
19:57420790:A:CQ433P0.991
19:57421347:T:CF619L0.991
19:57421349:T:AF619L0.991
19:57421349:T:GF619L0.991
19:57420255:T:CF255L0.990
19:57420257:C:AF255L0.990
19:57420257:C:GF255L0.990
19:57420786:C:GH432D0.990
19:57420956:T:AH488Q0.990
19:57420956:T:GH488Q0.990
19:57420958:A:CQ489P0.990
19:57420339:T:CF283L0.989
19:57420341:T:AF283L0.989
19:57420341:T:GF283L0.989
19:57420538:A:CQ349P0.989
19:57420954:C:GH488D0.989
19:57420507:T:CF339L0.988
19:57420509:T:AF339L0.988
19:57420509:T:GF339L0.988
19:57420704:T:AH404Q0.988
19:57420704:T:GH404Q0.988

dbSNP variants (sampled 300 via entrez): RS1000400318 (19:57414190 T>C), RS1000755043 (19:57412442 TAA>T), RS1000774038 (19:57419703 G>A), RS1001003663 (19:57413918 A>T), RS1001170822 (19:57417279 G>A,C), RS1001280690 (19:57411241 C>A,T), RS1001363243 (19:57418445 T>A), RS1001449104 (19:57416920 G>A), RS1002187054 (19:57417796 G>A,C), RS1002275343 (19:57412414 C>G,T), RS1002480799 (19:57412660 G>A), RS1002645763 (19:57417449 A>G), RS1002732895 (19:57410178 A>G), RS1002966800 (19:57421634 C>A,T), RS1003123889 (19:57415517 G>A)

Disease associations

OMIM: gene MIM:619254 | 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

21 total (human), top 21 by PubMed support.

ChemicalActions (top 5)PubMed papers
bisphenol Aincreases expression, affects cotreatment2
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
GSK-J4decreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
arseniteaffects binding, increases reaction1
manganese chlorideincreases abundance, increases expression1
ferrous chloridedecreases expression1
di-n-butylphosphoric acidaffects expression1
CGP 52608affects binding, increases reaction1
abrineincreases expression1
bisphenol Saffects cotreatment, increases expression1
Air Pollutantsaffects expression, increases abundance1
Atrazinedecreases expression1
Dexamethasoneaffects cotreatment, increases expression1
Indomethacinaffects cotreatment, increases expression1
Manganeseincreases abundance, increases expression1
Ozoneaffects expression, increases abundance1
Urethanedecreases expression1
1-Methyl-3-isobutylxanthineaffects cotreatment, increases expression1
Cadmium Chloridedecreases 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.