ZNF821

gene
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Summary

ZNF821 (zinc finger protein 821, HGNC:28043) is a protein-coding gene on chromosome 16q22.2, encoding Zinc finger protein 821 (O75541). May be involved in transcriptional regulation.

This gene encodes a protein with two C2H2 zinc finger motifs and a score-and-three (23)-amino acid peptide repeat (STPR) domain. The STPR domain of the encoded protein binds to double stranded DNA and may also contain a nuclear localization signal, suggesting that this protein interacts with chromosomal DNA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Source: NCBI Gene 55565 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 51 total
  • MANE Select transcript: NM_001201552

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28043
Approved symbolZNF821
Namezinc finger protein 821
Location16q22.2
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000102984
Ensembl biotypeprotein_coding
OMIM621289
Entrez55565

Gene structure

Transcript identifiers

Ensembl transcripts: 38 — 28 protein_coding, 6 nonsense_mediated_decay, 2 protein_coding_CDS_not_defined, 2 retained_intron

ENST00000313565, ENST00000425432, ENST00000446827, ENST00000561700, ENST00000562677, ENST00000562797, ENST00000562808, ENST00000562985, ENST00000563827, ENST00000563878, ENST00000564134, ENST00000564943, ENST00000565516, ENST00000565601, ENST00000565843, ENST00000566987, ENST00000568322, ENST00000568666, ENST00000568961, ENST00000569186, ENST00000611294, ENST00000861708, ENST00000861709, ENST00000861710, ENST00000861711, ENST00000861712, ENST00000861713, ENST00000861714, ENST00000861715, ENST00000861716, ENST00000918406, ENST00000918407, ENST00000918408, ENST00000918409, ENST00000918410, ENST00000918411, ENST00000958191, ENST00000958192

RefSeq mRNA: 11 — MANE Select: NM_001201552 NM_001201552, NM_001201553, NM_001201554, NM_001201556, NM_001318238, NM_001318239, NM_001376297, NM_001376298, NM_001376299, NM_001376300, NM_017530

CCDS: CCDS32481, CCDS56006, CCDS73911

Canonical transcript exons

ENST00000425432 — 8 exons

ExonStartEnd
ENSE000014054247188321171883273
ENSE000034963597185968571860672
ENSE000036491587186413871864242
ENSE000036715187186177671861942
ENSE000036850477187990771880023
ENSE000038445127188390871884182
ENSE000038910007186490371865048
ENSE000038932497186791271868037

Expression profiles

Bgee: expression breadth ubiquitous, 187 present calls, max score 95.77.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.8186 / max 71.7677, expressed in 1542 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
1580474.33361477
1580480.4851246

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
cortical plateUBERON:000534395.77gold quality
ganglionic eminenceUBERON:000402394.56gold quality
cerebellar hemisphereUBERON:000224591.74gold quality
cerebellar cortexUBERON:000212991.57gold quality
left testisUBERON:000453391.13gold quality
right hemisphere of cerebellumUBERON:001489091.09gold quality
right testisUBERON:000453490.85gold quality
cerebellumUBERON:000203789.84gold quality
ventricular zoneUBERON:000305389.78gold quality
testisUBERON:000047388.74gold quality
prefrontal cortexUBERON:000045185.62gold quality
adenohypophysisUBERON:000219685.25gold quality
oocyteCL:000002385.15gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047385.03gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099184.91gold quality
right frontal lobeUBERON:000281084.66gold quality
pituitary glandUBERON:000000784.41gold quality
cingulate cortexUBERON:000302782.87gold quality
embryoUBERON:000092282.79gold quality
anterior cingulate cortexUBERON:000983582.79gold quality
sural nerveUBERON:001548882.20gold quality
islet of LangerhansUBERON:000000682.18gold quality
tendon of biceps brachiiUBERON:000818882.17gold quality
Brodmann (1909) area 9UBERON:001354081.83gold quality
neocortexUBERON:000195081.50gold quality
skin of legUBERON:000151181.27gold quality
frontal cortexUBERON:000187080.96gold quality
dorsolateral prefrontal cortexUBERON:000983480.81gold quality
descending thoracic aortaUBERON:000234580.57gold quality
mucosa of transverse colonUBERON:000499180.48gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-CURD-10no56.15
E-ANND-3no3.07

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

17 targeting ZNF821, 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-6748-5P100.0065.811057
HSA-MIR-4747-5P100.0067.902681
HSA-MIR-5196-5P100.0067.982761
HSA-MIR-477599.9875.006394
HSA-MIR-6793-5P99.9765.95758
HSA-MIR-449299.8768.253611
HSA-MIR-6756-5P99.8267.972466
HSA-MIR-57799.7869.132479
HSA-MIR-674599.7465.331321
HSA-MIR-6766-5P99.6867.702325
HSA-MIR-363-5P99.4664.511015
HSA-MIR-6780B-3P99.1367.18622
HSA-MIR-448398.0964.121642
HSA-MIR-4793-5P96.8865.90872
HSA-MIR-129396.1664.69916
HSA-MIR-6815-5P96.0565.55662
HSA-MIR-6865-5P96.0565.58675

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_rerioznf821ENSDARG00000106989
mus_musculusZfp821ENSMUSG00000031728
rattus_norvegicusZfp821ENSRNOG00000000262
drosophila_melanogasterCG14442FBGN0029893
drosophila_melanogasterCG14440FBGN0029894

Paralogs (11): IKZF2 (ENSG00000030419), ZNF639 (ENSG00000121864), IKZF4 (ENSG00000123411), ZNF382 (ENSG00000161298), IKZF3 (ENSG00000161405), ZNF613 (ENSG00000176024), IKZF1 (ENSG00000185811), ZNF567 (ENSG00000189042), ZNF649 (ENSG00000198093), ZNF564 (ENSG00000249709), ZNF350 (ENSG00000256683)

Protein

Protein identifiers

Zinc finger protein 821O75541 (reviewed: O75541)

All UniProt accessions (11): O75541, A0A087WXX1, A0A0C4DH12, H3BPS7, H3BQE4, H3BR59, H3BR75, H3BRD6, H3BS68, H3BTZ4, H3BVG7

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?
O75541-11yes
O75541-22

RefSeq proteins (11): NP_001188481, NP_001188482, NP_001188483, NP_001188485, NP_001305167, NP_001305168, NP_001363226, NP_001363227, NP_001363228, NP_001363229, NP_060000 (=MANE)

Domains & families (InterPro)

IDNameType
IPR013087Znf_C2H2_typeDomain
IPR036236Znf_C2H2_sfHomologous_superfamily

UniProt features (8 total): zinc finger region 2, region of interest 2, chain 1, coiled-coil region 1, compositionally biased region 1, splice variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-O75541-F159.900.21

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 150 (showing top): chr16q22, CMYB_01, RACCACAR_AML_Q6, TAL1ALPHAE47_01, GGGTGGRR_PAX4_03, NFKB_C, MCAATNNNNNGCG_UNKNOWN, TSENG_IRS1_TARGETS_DN, MORF_BCL2L11, MODULE_95, TAL1BETAE47_01, GOCC_NUCLEAR_SPECK, GOCC_NUCLEAR_BODY, GOCC_RIBONUCLEOPROTEIN_GRANULE, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING

GO Biological Process (1): regulation of transcription by RNA polymerase II (GO:0006357)

GO Molecular Function (7): RNA polymerase II cis-regulatory region sequence-specific DNA binding (GO:0000978), DNA-binding transcription factor activity (GO:0003700), zinc ion binding (GO:0008270), sequence-specific double-stranded DNA binding (GO:1990837), DNA binding (GO:0003677), protein binding (GO:0005515), metal ion binding (GO:0046872)

GO Cellular Component (1): nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
regulation of DNA-templated transcription2
transcription by RNA polymerase II1
RNA polymerase II transcription regulatory region sequence-specific DNA binding1
cis-regulatory region sequence-specific DNA binding1
transcription cis-regulatory region binding1
transcription regulator activity1
transition metal ion binding1
double-stranded DNA binding1
sequence-specific DNA binding1
nucleic acid binding1
binding1
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

352 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF821ATXN1LP0C7T5597
ZNF821TRMT61AQ96FX7476
ZNF821RIN2Q8WYP3471
ZNF821TRMT6Q9UJA5470
ZNF821TXNL4BQ9NX01465
ZNF821DHX38Q92620430
ZNF821PMFBP1Q8TBY8426
ZNF821EGR4Q05215424
ZNF821ELF2Q15723420
ZNF821ZNF780AO75290391
ZNF821ZNF740Q8NDX6388
ZNF821ETV2O00321385
ZNF821NCAPD2Q15021379
ZNF821GOLGA6AQ9NYA3358
ZNF821MTHFSDQ2M296350

IntAct

16 interactions, top by confidence:

ABTypeScore
ZNF821CDCA7Lpsi-mi:“MI:0915”(physical association)0.560
PIM2ZNF821psi-mi:“MI:0915”(physical association)0.560
ZNF821PIM2psi-mi:“MI:0915”(physical association)0.560
CDCA7LZNF821psi-mi:“MI:0915”(physical association)0.560
ZNF821FXR1psi-mi:“MI:0915”(physical association)0.370
ZNF821SMARCA2psi-mi:“MI:0915”(physical association)0.370
ZNF821SPG11psi-mi:“MI:0915”(physical association)0.370
CCDC85BZNF821psi-mi:“MI:0915”(physical association)0.370
ZNF821LURAP1psi-mi:“MI:0915”(physical association)0.370
ATMZNF821psi-mi:“MI:0915”(physical association)0.370
S100A6VWA8psi-mi:“MI:0914”(association)0.350
MBD3L2AHCYL1psi-mi:“MI:0914”(association)0.350
NRIP1ZNF821psi-mi:“MI:0915”(physical association)0.000

BioGRID (14): ZNF821 (Two-hybrid), ZNF821 (Two-hybrid), ZNF821 (Two-hybrid), LURAP1 (Two-hybrid), ZNF821 (Two-hybrid), RUNDC3A (Two-hybrid), DVL3 (Two-hybrid), ZNF821 (Two-hybrid), ZNF821 (Two-hybrid), ZNF821 (Affinity Capture-MS), ZNF821 (Affinity Capture-MS), ZNF821 (Affinity Capture-MS), ZNF821 (Two-hybrid), ZWILCH (Cross-Linking-MS (XL-MS))

ESM2 similar proteins: A5PMU4, O60663, O75541, O88609, O97581, P29674, P36200, P48742, P50211, P50212, P50480, P50481, P52889, P53405, P53406, P53407, P53408, P53409, P53410, P53411, P53412, P53413, P53776, P61371, P61372, P61373, P61374, P61375, P61376, P63006, P63007, P63008, Q04650, Q32KS7, Q5IS44, Q5IS89, Q60564, Q6H8Q1, Q6KC51, Q6PD05

Diamond homologs: O57415, O75541, Q32KS7, Q3UH06, Q5NVT2, Q642B2, Q6IQ21, Q6PD05, Q8BIQ8, Q92766, Q96MM3, Q99LH4, O42409, O70237, P22227, P25490, Q00899, Q3TTC2, Q5VTD9, Q6DCW1, Q17R98, Q505G8, Q9BE73

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance44
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1749 predictions. Top by Δscore:

VariantEffectΔscore
16:71860668:TCTCA:Tacceptor_gain1.0000
16:71860669:CTCA:Cacceptor_gain1.0000
16:71860669:CTCAC:Cacceptor_gain1.0000
16:71860670:TCA:Tacceptor_gain1.0000
16:71860670:TCACT:Tacceptor_gain1.0000
16:71860671:CA:Cacceptor_gain1.0000
16:71860671:CAC:Cacceptor_gain1.0000
16:71860672:ACTG:Aacceptor_loss1.0000
16:71860673:C:CCacceptor_gain1.0000
16:71860673:C:CGacceptor_loss1.0000
16:71864985:T:TAdonor_gain1.0000
16:71879899:ATACT:Adonor_loss1.0000
16:71879901:ACT:Adonor_loss1.0000
16:71879902:CTC:Cdonor_loss1.0000
16:71879904:CA:Cdonor_loss1.0000
16:71879905:A:ACdonor_gain1.0000
16:71879905:ACA:Adonor_loss1.0000
16:71879906:C:CGdonor_gain1.0000
16:71879906:CA:Cdonor_gain1.0000
16:71879906:CAGTG:Cdonor_gain1.0000
16:71880019:CTAAC:Cacceptor_gain1.0000
16:71880020:TAAC:Tacceptor_gain1.0000
16:71880021:AAC:Aacceptor_gain1.0000
16:71880021:AACC:Aacceptor_loss1.0000
16:71880022:AC:Aacceptor_gain1.0000
16:71880023:CC:Cacceptor_gain1.0000
16:71880024:C:CAacceptor_loss1.0000
16:71880024:C:CCacceptor_gain1.0000
16:71880025:T:Cacceptor_loss1.0000
16:71883183:G:Cdonor_gain1.0000

AlphaMissense

2712 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:71860195:C:AR354S1.000
16:71860195:C:GR354S1.000
16:71860207:C:AK350N1.000
16:71860207:C:GK350N1.000
16:71860209:T:CK350E1.000
16:71860212:C:GA349P1.000
16:71860217:C:GR347P1.000
16:71860221:C:TE346K1.000
16:71860223:C:GR345P1.000
16:71860229:A:GL343P1.000
16:71860281:C:GA326P1.000
16:71860292:C:GR322P1.000
16:71860298:A:GL320P1.000
16:71860335:G:TR308S1.000
16:71860345:C:AK304N1.000
16:71860345:C:GK304N1.000
16:71860347:T:CK304E1.000
16:71860370:C:AR296M1.000
16:71861822:A:GC180R1.000
16:71861854:A:GL169P1.000
16:71861856:G:CH168Q1.000
16:71861856:G:TH168Q1.000
16:71861857:T:CH168R1.000
16:71861858:G:CH168D1.000
16:71861858:G:TH168N1.000
16:71861895:A:CC155W1.000
16:71861896:C:TC155Y1.000
16:71861897:A:GC155R1.000
16:71861904:A:CC152W1.000
16:71861906:A:GC152R1.000

dbSNP variants (sampled 300 via entrez): RS1000083044 (16:71860637 A>G,T), RS1000088789 (16:71889386 A>G), RS1000283993 (16:71884083 C>T), RS1000287692 (16:71895226 G>A), RS1000328821 (16:71890110 A>C), RS1000373897 (16:71861543 T>C), RS1000448127 (16:71862081 GA>G), RS1000649436 (16:71884858 T>G), RS1000660385 (16:71891431 C>G,T), RS1000693730 (16:71873726 T>G), RS1000743611 (16:71861200 C>A), RS1001020240 (16:71885115 C>A,G,T), RS1001051097 (16:71884914 A>G), RS1001100767 (16:71890936 A>C), RS1001145212 (16:71873939 G>A,C)

Disease associations

OMIM: gene MIM:621289 | 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

24 total (human), top 24 by PubMed support.

ChemicalActions (top 5)PubMed papers
Particulate Matterdecreases expression, increases abundance2
alpha-pineneaffects cotreatment, increases expression, increases abundance1
bisphenol Aaffects cotreatment, increases expression1
afimoxifenedecreases expression, decreases reaction1
tris(1,3-dichloro-2-propyl)phosphateincreases expression1
methacrylaldehydeincreases abundance, affects cotreatment, increases expression1
abrineincreases expression1
Acroleinaffects cotreatment, increases expression, increases abundance1
Air Pollutantsincreases abundance, increases expression, affects cotreatment1
Arsenicaffects methylation1
Vehicle Emissionsdecreases expression, increases abundance1
Dexamethasoneaffects cotreatment, increases expression1
Estradioldecreases expression1
Estrogensdecreases expression, decreases reaction1
Gallic Aciddecreases expression1
Indomethacinaffects cotreatment, increases expression1
Ozoneaffects cotreatment, increases expression, increases abundance1
Phthalic Acidsincreases methylation1
Tobacco Smoke Pollutiondecreases expression1
Urethanedecreases expression, increases expression1
Zincdecreases expression1
1-Methyl-3-isobutylxanthineaffects cotreatment, increases expression1
Okadaic Aciddecreases expression1
Volatile Organic Compoundsincreases expression, affects cotreatment1

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.