ZNF19

gene
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Also known as KOX12MGC51021

Summary

ZNF19 (zinc finger protein 19, HGNC:12981) is a protein-coding gene on chromosome 16q22.2, encoding Zinc finger protein 19 (P17023). May be involved in transcriptional regulation.

The protein encoded by this gene contains a zinc finger, a nucleic acid-binding domain present in many transcription factors. This gene is located in a region next to ZNF23, a gene also encoding a zinc finger protein, on chromosome 16.

Source: NCBI Gene 7567 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 60 total
  • MANE Select transcript: NM_006961

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12981
Approved symbolZNF19
Namezinc finger protein 19
Location16q22.2
Locus typegene with protein product
StatusApproved
AliasesKOX12, MGC51021
Ensembl geneENSG00000157429
Ensembl biotypeprotein_coding
OMIM194525
Entrez7567

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 14 protein_coding, 2 nonsense_mediated_decay, 2 protein_coding_CDS_not_defined, 1 retained_intron

ENST00000288177, ENST00000561469, ENST00000562210, ENST00000564225, ENST00000564230, ENST00000565100, ENST00000565541, ENST00000565637, ENST00000566202, ENST00000567225, ENST00000568446, ENST00000568815, ENST00000569072, ENST00000569717, ENST00000617615, ENST00000866316, ENST00000866317, ENST00000866318, ENST00000948558

RefSeq mRNA: 1 — MANE Select: NM_006961 NM_006961

CCDS: CCDS10901

Canonical transcript exons

ENST00000288177 — 6 exons

ExonStartEnd
ENSE000011060087147358371476272
ENSE000013516467148927271489324
ENSE000034590657147822871478341
ENSE000034897947147887971479005
ENSE000035690927148458971484748
ENSE000036707527148208271482143

Expression profiles

Bgee: expression breadth ubiquitous, 189 present calls, max score 91.07.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 3.6087 / max 75.5710, expressed in 1279 samples.

FANTOM5 promoters (5 alternative TSS)

Promoter IDTPM avgSamples expressed
1580072.02801115
1580101.0097398
1580060.549081
1580080.01463
1580090.00743

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right uterine tubeUBERON:000130291.07gold quality
ileal mucosaUBERON:000033182.78silver quality
pancreatic ductal cellCL:000207982.69silver quality
tibialis anteriorUBERON:000138582.65silver quality
right testisUBERON:000453481.75gold quality
left testisUBERON:000453381.51gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099181.50gold quality
adenohypophysisUBERON:000219680.96gold quality
testisUBERON:000047380.40gold quality
pituitary glandUBERON:000000780.24gold quality
right lobe of thyroid glandUBERON:000111980.22gold quality
left lobe of thyroid glandUBERON:000112080.09gold quality
thyroid glandUBERON:000204679.62gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047378.87gold quality
bronchial epithelial cellCL:000232878.72gold quality
mucosa of paranasal sinusUBERON:000503078.10silver quality
sural nerveUBERON:001548877.91gold quality
bronchusUBERON:000218577.71gold quality
olfactory segment of nasal mucosaUBERON:000538676.93gold quality
islet of LangerhansUBERON:000000676.56gold quality
metanephrosUBERON:000008176.34gold quality
ventricular zoneUBERON:000305376.34gold quality
fallopian tubeUBERON:000388976.24gold quality
colonic epitheliumUBERON:000039775.86gold quality
right lungUBERON:000216775.58gold quality
metanephros cortexUBERON:001053375.54gold quality
body of pancreasUBERON:000115075.32gold quality
cortical plateUBERON:000534374.99gold quality
pancreasUBERON:000126474.94gold quality
oviduct epitheliumUBERON:000480474.13gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): STAT1

miRNA regulators (miRDB)

48 targeting ZNF19, 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-499A-5P99.9870.791323
HSA-MIR-1229-3P99.9766.49906
HSA-MIR-548AA99.9670.643753
HSA-MIR-548AP-3P99.9670.643753
HSA-MIR-548T-3P99.9670.643753
HSA-MIR-10523-5P99.9169.222038
HSA-MIR-808799.9069.551351
HSA-MIR-1343-3P99.8966.781815
HSA-MIR-6783-3P99.8967.922059
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-548AZ-3P99.8270.563549
HSA-MIR-548BC99.8270.613524
HSA-MIR-548E-3P99.8270.593514
HSA-MIR-548F-3P99.8270.593540
HSA-MIR-7110-5P99.8067.841712
HSA-MIR-548A-3P99.7670.583524
HSA-MIR-187-5P99.7470.261404
HSA-MIR-120099.7170.421838
HSA-MIR-120899.7068.281533
HSA-MIR-7157-5P99.6669.331829
HSA-MIR-368599.6268.831621
HSA-MIR-431099.5968.842527
HSA-MIR-888-3P99.5369.771057
HSA-MIR-154-3P99.5070.05831
HSA-MIR-487A-3P99.5069.95840
HSA-MIR-442799.3470.331854
HSA-MIR-1273H-3P99.2967.55980
HSA-MIR-6731-5P99.2867.422375
HSA-MIR-548AS-3P99.1269.122294
HSA-MIR-4711-3P98.9766.871020

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
drosophila_melanogasterCG2712FBGN0024975
drosophila_melanogasterPhsFBGN0036522
drosophila_melanogasterCG3281FBGN0260741

Paralogs (62): ZNF582 (ENSG00000018869), ZNF264 (ENSG00000083844), ZNF343 (ENSG00000088876), ZNF684 (ENSG00000117010), ZNF133 (ENSG00000125846), ZNF557 (ENSG00000130544), ZNF337 (ENSG00000130684), ZNF20 (ENSG00000132010), ZFP37 (ENSG00000136866), ZNF614 (ENSG00000142556), KRBOX4 (ENSG00000147121), ZNF599 (ENSG00000153896), ZNF589 (ENSG00000164048), PRDM9 (ENSG00000164256), ZNF180 (ENSG00000167384), ZNF558 (ENSG00000167785), ZNF35 (ENSG00000169981), ZNF778 (ENSG00000170100), ZNF439 (ENSG00000171291), ZNF440 (ENSG00000171295), ZNF556 (ENSG00000172000), ZNF554 (ENSG00000172006), ZNF596 (ENSG00000172748), ZNF80 (ENSG00000174255), ZNF266 (ENSG00000174652), ZNF25 (ENSG00000175395), ZNF77 (ENSG00000175691), ZNF169 (ENSG00000175787), ZNF404 (ENSG00000176222), ZNF491 (ENSG00000177599), ZNF620 (ENSG00000177842), ZNF619 (ENSG00000177873), ZNF875 (ENSG00000181666), ZNF329 (ENSG00000181894), ZFP90 (ENSG00000184939), ZNF566 (ENSG00000186017), ZNF529 (ENSG00000186020), ZNF749 (ENSG00000186230), ZNF555 (ENSG00000186300), ZNF70 (ENSG00000187792)

Protein

Protein identifiers

Zinc finger protein 19P17023 (reviewed: P17023)

Alternative names: Zinc finger protein KOX12

All UniProt accessions (10): P17023, H3BMU5, H3BNH9, H3BNI0, H3BQ26, H3BQI6, H3BR98, J3KRI7, J3KSN3, J3KT56

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 (2)

UniProt IDNamesCanonical?
P17023-11yes
P17023-22

RefSeq proteins (1): NP_008892* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050589Ikaros_C2H2-ZFFamily

Pfam: PF00096, PF01352

UniProt features (17 total): zinc finger region 10, sequence variant 2, sequence conflict 2, chain 1, domain 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P17023-F171.760.13

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 33 (showing top): chr16q22, XU_GH1_EXOGENOUS_TARGETS_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, DODD_NASOPHARYNGEAL_CARCINOMA_DN, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, BCL6B_TARGET_GENES, CENPT_TARGET_GENES, CSHL1_TARGET_GENES, DLX4_TARGET_GENES, FOXN3_TARGET_GENES, SNIP1_TARGET_GENES, TERF1_TARGET_GENES, ZIM3_TARGET_GENES, ZNF410_TARGET_GENES, MIR4310

GO Biological Process (2): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355)

GO Molecular Function (7): RNA polymerase II transcription regulatory region sequence-specific DNA binding (GO:0000977), 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), sequence-specific double-stranded DNA binding (GO:1990837)

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 DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
transcription cis-regulatory region binding1
chromatin1
RNA polymerase II transcription regulatory region sequence-specific DNA binding1
DNA-binding transcription factor activity1
regulation of transcription by RNA polymerase II1
transition metal ion binding1
nucleic acid binding1
binding1
cation binding1
double-stranded DNA binding1
sequence-specific DNA binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

518 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF19NOX4Q9NPH5772
ZNF19TTC39AQ5SRH9543
ZNF19CCDC71Q8IV32490
ZNF19CREB5Q02930464
ZNF19NIPAL2Q9H841450
ZNF19LEMD3Q9Y2U8443
ZNF19TMBIM4Q9HC24442
ZNF19SPDYE6P0CI01434
ZNF19ZNF292O60281422
ZNF19KLF11O14901411
ZNF19FRA10AC1Q70Z53399
ZNF19MEPEQ9NQ76391
ZNF19SNAI2O43623379
ZNF19C1orf21Q9H246377
ZNF19NBPF20P0DPF2373

IntAct

88 interactions, top by confidence:

ABTypeScore
CTNNA3ZNF19psi-mi:“MI:0915”(physical association)0.560
CSNK2BZNF19psi-mi:“MI:0915”(physical association)0.560
CDR2LZNF19psi-mi:“MI:0915”(physical association)0.560
FAM72DZNF19psi-mi:“MI:0915”(physical association)0.560
LMO2ZNF19psi-mi:“MI:0915”(physical association)0.560
SCNM1ZNF19psi-mi:“MI:0915”(physical association)0.560
MAGOHBZNF19psi-mi:“MI:0915”(physical association)0.560
LMO1ZNF19psi-mi:“MI:0915”(physical association)0.560
NUDT22ZNF19psi-mi:“MI:0915”(physical association)0.560
CINPZNF19psi-mi:“MI:0915”(physical association)0.560
ZNF417ZNF19psi-mi:“MI:0915”(physical association)0.560
BCCIPZNF19psi-mi:“MI:0915”(physical association)0.560
BEX2ZNF19psi-mi:“MI:0915”(physical association)0.560
CARD9ZNF19psi-mi:“MI:0915”(physical association)0.560
NDUFAB1ZNF19psi-mi:“MI:0915”(physical association)0.560
ZNF19RFC5psi-mi:“MI:0915”(physical association)0.560
ZNF19SPANXN2psi-mi:“MI:0915”(physical association)0.560
ZNF19ZNF417psi-mi:“MI:0915”(physical association)0.560
ZNF19AP1M1psi-mi:“MI:0915”(physical association)0.560
ZNF19ATPAF2psi-mi:“MI:0915”(physical association)0.560

BioGRID (30): TRIM28 (Affinity Capture-MS), TRIM39 (Affinity Capture-MS), TRIM39 (Affinity Capture-MS), TRIM28 (Affinity Capture-MS), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid), ZNF19 (Two-hybrid)

ESM2 similar proteins: A1L1L7, A3KN36, D3ZVT0, O43296, P08042, P13682, P16373, P17023, P17097, P52738, P85977, Q02975, Q12901, Q14590, Q14592, Q2M3W8, Q2VY69, Q4V8A8, Q571J5, Q5CZA5, Q5R7I8, Q5RB33, Q5RBX0, Q61751, Q61967, Q6GQR8, Q6PF04, Q6ZNG0, Q6ZS27, Q86Y25, Q8BFS8, Q8BQC8, Q8IZ26, Q8N782, Q8N9Z0, Q8R1D1, Q8TF47, Q8WTR7, Q96LW1, Q9BS31

Diamond homologs: A0JPL0, A1L1L7, A2A761, A2VDP4, A3KN36, A6QLU5, A6QPT6, A7MBI1, A8MT65, B2RXC5, E9PYI1, E9Q8G5, O75290, O94892, O95780, P10076, P17014, P17023, P17025, P17030, P17032, P17098, P51523, P51814, P52736, P52742, P58317, Q02975, Q06730, Q06732, Q08DG8, Q0VCB0, Q13360, Q14584, Q14587, Q14590, Q147U1, Q16587, Q29RZ4, Q2M218

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance57
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1675 predictions. Top by Δscore:

VariantEffectΔscore
16:71478224:CTA:Cdonor_loss1.0000
16:71478225:TA:Tdonor_loss1.0000
16:71478226:A:ATdonor_loss1.0000
16:71478227:C:CTdonor_loss1.0000
16:71478340:CC:Cacceptor_gain1.0000
16:71478341:CC:Cacceptor_gain1.0000
16:71478342:C:CCacceptor_gain1.0000
16:71525376:G:GTdonor_gain1.0000
16:71476091:TGGA:Tdonor_gain0.9900
16:71476100:T:Adonor_gain0.9900
16:71476270:CAT:Cacceptor_gain0.9900
16:71476271:ATCTG:Aacceptor_loss0.9900
16:71476273:C:Aacceptor_loss0.9900
16:71476277:C:CTacceptor_gain0.9900
16:71476278:A:Cacceptor_gain0.9900
16:71478338:TACC:Tacceptor_gain0.9900
16:71478340:CCCT:Cacceptor_loss0.9900
16:71478342:C:CAacceptor_loss0.9900
16:71478343:T:Aacceptor_loss0.9900
16:71478872:GCCTT:Gdonor_loss0.9900
16:71478873:CCTTA:Cdonor_loss0.9900
16:71478874:CTT:Cdonor_loss0.9900
16:71478875:TTA:Tdonor_loss0.9900
16:71478875:TTAC:Tdonor_loss0.9900
16:71478876:TA:Tdonor_loss0.9900
16:71478877:AC:Adonor_gain0.9900
16:71478877:ACCC:Adonor_loss0.9900
16:71478878:CC:Cdonor_gain0.9900
16:71484750:T:Cacceptor_gain0.9900
16:71488965:C:Adonor_gain0.9900

AlphaMissense

3062 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:71475701:A:CF282L0.998
16:71475701:A:TF282L0.998
16:71475703:A:GF282L0.998
16:71475869:A:CF226L0.998
16:71475869:A:TF226L0.998
16:71475871:A:GF226L0.998
16:71475953:A:CF198L0.998
16:71475953:A:TF198L0.998
16:71475955:A:GF198L0.998
16:71475533:G:CF338L0.997
16:71475533:G:TF338L0.997
16:71475535:A:GF338L0.997
16:71475617:A:CF310L0.997
16:71475617:A:TF310L0.997
16:71475619:A:GF310L0.997
16:71475785:G:CF254L0.997
16:71475785:G:TF254L0.997
16:71475787:A:GF254L0.997
16:71475585:C:GR321P0.996
16:71475756:T:GQ264P0.996
16:71475842:A:CH235Q0.996
16:71475842:A:TH235Q0.996
16:71475844:G:CH235D0.996
16:71475852:A:GL232P0.996
16:71475449:G:CF366L0.995
16:71475449:G:TF366L0.995
16:71475451:A:GF366L0.995
16:71475600:A:GL316P0.995
16:71475674:A:CH291Q0.995
16:71475674:A:TH291Q0.995

dbSNP variants (sampled 300 via entrez): RS1000058973 (16:71488985 C>G,T), RS1000300451 (16:71488579 G>A,C), RS1000317683 (16:71488343 G>A,T), RS1000328498 (16:71488681 C>T), RS1000532036 (16:71477145 G>T), RS1000928887 (16:71490070 A>C,T), RS1001022300 (16:71490335 T>C), RS1001052893 (16:71477446 T>C), RS1001118780 (16:71484034 C>A,T), RS1001231214 (16:71489331 C>A,G), RS1001464933 (16:71490512 T>C), RS1001599068 (16:71489602 G>A), RS1001607316 (16:71474251 C>T), RS1001639544 (16:71487292 G>A), RS1001693596 (16:71487575 A>G)

Disease associations

OMIM: gene MIM:194525 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

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

GWAS associations

1 associations (top):

StudyTraitp-value
GCST005316_209Intelligence (MTAG)2.000000e-08

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004337intelligence

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

22 total (human), top 22 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases methylation2
Esketaminedecreases expression1
methylmercuric chloridedecreases expression1
terbufosdecreases methylation1
trichostatin Adecreases expression1
sodium arsenitedecreases expression1
ferrous chloridedecreases expression1
perfluorooctane sulfonic acidincreases expression1
CGP 52608increases reaction, affects binding1
abrineincreases expression1
Sunitinibincreases expression1
Arsenic Trioxidedecreases expression1
Leflunomideincreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Cisplatinincreases expression1
Doxorubicindecreases expression1
Fonofosdecreases methylation1
Parathiondecreases methylation1
Thiramdecreases expression1
Tobacco Smoke Pollutiondecreases expression1
Urethanedecreases expression1
Okadaic Aciddecreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_XW14HEK293 eGFP-ZNF19Transformed 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.