ZNF791

gene
On this page

Also known as FLJ90396

Summary

ZNF791 (zinc finger protein 791, HGNC:26895) is a protein-coding gene on chromosome 19p13.13, encoding Zinc finger protein 791 (Q3KP31). May be involved in transcriptional regulation.

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription 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 163049 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 58 total
  • MANE Select transcript: NM_153358

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26895
Approved symbolZNF791
Namezinc finger protein 791
Location19p13.13
Locus typegene with protein product
StatusApproved
AliasesFLJ90396
Ensembl geneENSG00000173875
Ensembl biotypeprotein_coding
Entrez163049

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 3 protein_coding, 2 nonsense_mediated_decay, 1 protein_coding_CDS_not_defined

ENST00000343325, ENST00000446165, ENST00000498389, ENST00000597691, ENST00000598225, ENST00000600752

RefSeq mRNA: 1 — MANE Select: NM_153358 NM_153358

CCDS: CCDS12273

Canonical transcript exons

ENST00000343325 — 4 exons

ExonStartEnd
ENSE000014022631262772112633834
ENSE000035930311261092012611082
ENSE000036441881262465012624710
ENSE000036614911262370012623826

Expression profiles

Bgee: expression breadth ubiquitous, 256 present calls, max score 95.82.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 25.1223 / max 355.6993, expressed in 1804 samples.

FANTOM5 promoters (4 alternative TSS)

Promoter IDTPM avgSamples expressed
17399518.71671797
1739973.44531193
1739962.83741375
1739990.123047

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
nippleUBERON:000203095.82gold quality
pylorusUBERON:000116694.54gold quality
pericardiumUBERON:000240794.25gold quality
superior surface of tongueUBERON:000737193.75gold quality
renal medullaUBERON:000036293.67gold quality
calcaneal tendonUBERON:000370193.61gold quality
tracheaUBERON:000312693.50gold quality
trigeminal ganglionUBERON:000167593.41gold quality
inferior vagus X ganglionUBERON:000536393.28gold quality
cardiac muscle of right atriumUBERON:000337992.65gold quality
cardia of stomachUBERON:000116292.57gold quality
ventral tegmental areaUBERON:000269192.26gold quality
left ventricle myocardiumUBERON:000656691.98gold quality
saphenous veinUBERON:000731891.69gold quality
pancreatic ductal cellCL:000207991.60gold quality
medulla oblongataUBERON:000189691.57gold quality
dorsal root ganglionUBERON:000004491.36gold quality
ileal mucosaUBERON:000033191.34gold quality
seminal vesicleUBERON:000099891.21gold quality
layer of synovial tissueUBERON:000761691.10gold quality
mammary ductUBERON:000176590.94gold quality
subthalamic nucleusUBERON:000190690.93gold quality
kidney epitheliumUBERON:000481990.93gold quality
epithelium of mammary glandUBERON:000324490.92gold quality
superior vestibular nucleusUBERON:000722790.88gold quality
urethraUBERON:000005790.61gold quality
dorsal plus ventral thalamusUBERON:000189790.56gold quality
cartilage tissueUBERON:000241890.27gold quality
sural nerveUBERON:001548890.19gold quality
corpus callosumUBERON:000233690.12gold quality

Single-cell (SCXA)

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

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

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

22 targeting ZNF791, 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-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-6873-3P100.0071.422626
HSA-MIR-150-5P99.9966.691976
HSA-MIR-6778-3P99.9667.292693
HSA-MIR-971899.9468.91918
HSA-MIR-568099.9169.833421
HSA-MIR-6515-3P99.8268.191933
HSA-MIR-494-3P99.7071.452795
HSA-MIR-427999.1966.702437
HSA-MIR-3944-5P98.5067.55997
HSA-MIR-628-5P98.3667.74844
HSA-MIR-6742-3P97.9564.501490
HSA-MIR-193B-5P97.9165.88837
HSA-MIR-15B-3P97.8566.68974
HSA-MIR-1226-3P97.5166.321063
HSA-MIR-194-3P97.3665.961027
HSA-MIR-64397.3567.91805
HSA-MIR-4793-3P94.8765.85896
HSA-MIR-431594.7864.86112
HSA-MIR-4694-5P94.6265.39532
HSA-MIR-6890-5P92.8965.83442

Literature-anchored findings (GeneRIF, showing 1)

  • LncRNA KCNQ1OT1 contributes to hydrogen peroxide-induced apoptosis, inflammation, and oxidative stress of cardiomyocytes via miR-130a-3p/ZNF791 axis. (PMID:35989482)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusZfp791ENSMUSG00000074194
rattus_norvegicusZfp791ENSRNOG00000023920

Paralogs (15): ZNF14 (ENSG00000105708), ZNF57 (ENSG00000171970), ZNF443 (ENSG00000180855), ZNF101 (ENSG00000181896), ZNF563 (ENSG00000188868), ZNF799 (ENSG00000196466), ZNF700 (ENSG00000196757), ZNF441 (ENSG00000197044), ZNF433 (ENSG00000197647), ZNF44 (ENSG00000197857), ZNF823 (ENSG00000197933), ZNF442 (ENSG00000198342), ZNF844 (ENSG00000223547), ZNF709 (ENSG00000242852), ZNF878 (ENSG00000257446)

Protein

Protein identifiers

Zinc finger protein 791Q3KP31 (reviewed: Q3KP31)

All UniProt accessions (5): Q3KP31, C9JU55, M0QYQ0, M0R0E8, M0R2N1

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?
Q3KP31-11yes
Q3KP31-22

RefSeq proteins (1): NP_699189* (*=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 (21 total): zinc finger region 17, chain 1, domain 1, splice variant 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q3KP31-F181.260.40

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 53 (showing top): ACEVEDO_LIVER_CANCER_UP, OSMAN_BLADDER_CANCER_DN, chr19p13, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, ALKBH3_TARGET_GENES, CIITA_TARGET_GENES, DIDO1_TARGET_GENES, ELF2_TARGET_GENES, HES4_TARGET_GENES, PAX3_TARGET_GENES, RORA_TARGET_GENES, ZNF146_TARGET_GENES, ZNF274_TARGET_GENES, ZNF30_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 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)

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
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

578 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF791OR4F21O95013444
ZNF791ZNF487B1APH4431
ZNF791GARIN5AQ6IPT2418
ZNF791TMCO6Q96DC7401
ZNF791RNF208Q9H0X6348
ZNF791PAXBP1Q9Y5B6313
ZNF791POGZQ7Z3K3310
ZNF791EIF4E1BA6NMX2310
ZNF791HUS1BQ8NHY5310
ZNF791ZGLP1P0C6A0297
ZNF791OR51B4Q9Y5P0290
ZNF791ETFBKMTQ8IXQ9289
ZNF791MRPS11P82912287
ZNF791WFDC5Q8TCV5284
ZNF791KLHDC7BQ96G42278

IntAct

30 interactions, top by confidence:

ABTypeScore
GRNZNF791psi-mi:“MI:0915”(physical association)0.560
ZNF791WFS1psi-mi:“MI:0915”(physical association)0.560
HRCZNF791psi-mi:“MI:0914”(association)0.530
RPS3ZNF316psi-mi:“MI:0914”(association)0.530
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
EFEMP1ZNF316psi-mi:“MI:0914”(association)0.350
Mpsi-mi:“MI:0914”(association)0.350
PURGZNF320psi-mi:“MI:0914”(association)0.350
ZNF467ZNF320psi-mi:“MI:0914”(association)0.350
NOP2ZNF320psi-mi:“MI:0914”(association)0.350
NOTCH2ZNF320psi-mi:“MI:0914”(association)0.350
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
RPL36GTPBP10psi-mi:“MI:0914”(association)0.350
RPL13AGTPBP10psi-mi:“MI:0914”(association)0.350
TEX19ZNF316psi-mi:“MI:0914”(association)0.350
GLI4ZNF316psi-mi:“MI:0914”(association)0.350
KRT40ANKRD36psi-mi:“MI:0914”(association)0.350
SURF6psi-mi:“MI:0914”(association)0.350
APPZNF724psi-mi:“MI:0914”(association)0.350
PRKRAMPHOSPH10psi-mi:“MI:0914”(association)0.350
PRKRAGTPBP10psi-mi:“MI:0914”(association)0.350
RPL13POLRMTpsi-mi:“MI:0914”(association)0.350
ZNF791psi-mi:“MI:0915”(physical association)0.000

BioGRID (24): ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS), ZNF791 (Affinity Capture-MS)

ESM2 similar proteins: A6NK75, C9JN71, O75820, O94892, P08043, P0CJ79, P16415, P17017, P17021, P17035, P17039, P35789, P52737, Q08AN1, Q3KP31, Q3ZCX4, Q4R4C7, Q52M93, Q5MCW4, Q5R9F0, Q5RB30, Q5RDX1, Q5REA0, Q5REI6, Q5REK1, Q6P3V2, Q6ZN19, Q6ZNA1, Q6ZNG1, Q76KX8, Q80W31, Q86T29, Q86YE8, Q8C827, Q8N4W9, Q8N7K0, Q8NB50, Q8NDQ6, Q8NEP9, Q8TBZ8

Diamond homologs: A0JPK3, A8MT65, C9JN71, E9QAG8, G3X9G7, O75820, P16373, P16374, P16415, P17017, P17024, P17025, P51815, P52737, Q08AG5, Q08ER8, Q0D2J5, Q15973, Q2M218, Q3KP31, Q3V080, Q494X3, Q4R4C7, Q5MYW4, Q5R9F0, Q5R9S5, Q5REI6, Q5REK1, Q68EA5, Q6P560, Q6P5C7, Q6ZQV5, Q7L945, Q86T29, Q8BGV5, Q8C6P8, Q8IYI8, Q8IZC7, Q8N7K0, Q8N972

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 28 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
Major pathway of rRNA processing in the nucleolus and cytosol515.4×4e-04

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance47
Likely benign8
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

507 predictions. Top by Δscore:

VariantEffectΔscore
19:12611080:ATGG:Adonor_loss1.0000
19:12611081:TGG:Tdonor_loss1.0000
19:12611084:T:Adonor_loss1.0000
19:12623684:ATATT:Aacceptor_gain1.0000
19:12623685:T:Gacceptor_gain1.0000
19:12623686:A:AGacceptor_gain1.0000
19:12623686:ATT:Aacceptor_gain1.0000
19:12623686:ATTG:Aacceptor_gain1.0000
19:12623687:T:Gacceptor_gain1.0000
19:12623688:T:TAacceptor_gain1.0000
19:12623689:G:Aacceptor_gain1.0000
19:12623692:T:Aacceptor_gain1.0000
19:12623695:TTCA:Tacceptor_loss1.0000
19:12623696:TCA:Tacceptor_loss1.0000
19:12623696:TCAGG:Tacceptor_gain1.0000
19:12623697:CAGGA:Cacceptor_gain1.0000
19:12623698:A:AGacceptor_gain1.0000
19:12623698:AG:Aacceptor_gain1.0000
19:12623699:G:GCacceptor_gain1.0000
19:12623699:GG:Gacceptor_gain1.0000
19:12623699:GGA:Gacceptor_gain1.0000
19:12623699:GGAC:Gacceptor_gain1.0000
19:12623699:GGACT:Gacceptor_gain1.0000
19:12623822:TATAG:Tdonor_gain1.0000
19:12623823:ATAG:Adonor_gain1.0000
19:12623823:ATAGG:Adonor_loss1.0000
19:12623824:TAG:Tdonor_gain1.0000
19:12623824:TAGGT:Tdonor_loss1.0000
19:12623825:AG:Adonor_gain1.0000
19:12623825:AGG:Adonor_loss1.0000

AlphaMissense

3855 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:12628202:T:CF225L0.993
19:12628204:C:AF225L0.993
19:12628204:C:GF225L0.993
19:12628622:T:CF365L0.990
19:12628624:T:AF365L0.990
19:12628624:T:GF365L0.990
19:12628958:T:CF477L0.990
19:12628960:T:AF477L0.990
19:12628960:T:GF477L0.990
19:12629042:T:CF505L0.989
19:12629044:T:AF505L0.989
19:12629044:T:GF505L0.989
19:12628538:T:CF337L0.988
19:12628540:C:AF337L0.988
19:12628540:C:GF337L0.988
19:12628286:T:CF253L0.986
19:12628288:C:AF253L0.986
19:12628288:C:GF253L0.986
19:12629126:T:CF533L0.985
19:12629128:T:AF533L0.985
19:12629128:T:GF533L0.985
19:12628370:T:CF281L0.984
19:12628372:C:AF281L0.984
19:12628372:C:GF281L0.984
19:12628874:T:CF449L0.984
19:12628876:C:AF449L0.984
19:12628876:C:GF449L0.984
19:12628706:T:CF393L0.983
19:12628708:C:AF393L0.983
19:12628708:C:GF393L0.983

dbSNP variants (sampled 300 via entrez): RS1000134915 (19:12620024 C>A,T), RS1000362989 (19:12611378 C>T), RS1000786455 (19:12631551 G>A), RS1000966271 (19:12631849 G>A,C,T), RS1001103957 (19:12616043 T>C), RS1001225814 (19:12617073 A>G), RS1001248729 (19:12627876 C>G,T), RS1001276630 (19:12616828 T>A,G), RS1001353668 (19:12610334 G>A), RS1001414251 (19:12622156 A>G), RS1001519110 (19:12615280 C>T), RS1001545035 (19:12618915 T>G), RS1001613450 (19:12622717 A>C), RS1001635176 (19:12615556 G>A), RS1001876381 (19:12633174 T>C)

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

33 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Air Pollutantsaffects cotreatment, decreases expression, increases abundance, affects expression4
sodium arseniteincreases abundance, increases expression2
Ozonedecreases expression, increases abundance, affects expression, affects cotreatment2
Smokedecreases expression, increases abundance2
Tobacco Smoke Pollutionaffects expression, increases expression2
3-((6-(2-methoxyphenyl)pyrimidin-4-yl)amino)phenyl)methane sulfonamidedecreases expression1
TAK-243increases sumoylation1
triphenyl phosphateaffects expression1
alpha-pinenedecreases expression, increases abundance, affects cotreatment1
bisphenol Aaffects expression1
potassium chromate(VI)increases expression, affects cotreatment1
methacrylaldehydeincreases abundance, affects cotreatment, decreases expression1
epigallocatechin gallateaffects cotreatment, increases expression1
K 7174increases expression1
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II)decreases expression1
jinfukangaffects cotreatment, decreases expression1
Resveratrolaffects cotreatment, increases expression1
Acroleindecreases expression, increases abundance, affects cotreatment1
Arsenicincreases expression, increases abundance1
Cisplatinaffects cotreatment, decreases expression1
Coaldecreases expression, increases abundance1
Dietary Carbohydratesdecreases expression1
Doxorubicindecreases expression1
Plant Extractsaffects cotreatment, increases expression1
Urethaneincreases expression1
Valproic Acidincreases expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases expression1
Aflatoxin M1decreases expression1
Cadmium Chloridedecreases expression1
Copper Sulfateincreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

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

CellosaurusNameCategorySex
CVCL_XW87HEK293 eGFP-ZNF791Transformed 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.