ZNF33B

gene
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Also known as KOX31KOX2

Summary

ZNF33B (zinc finger protein 33B, HGNC:13097) is a protein-coding gene on chromosome 10q11.21, encoding Zinc finger protein 33B (Q06732). May be involved in transcriptional regulation.

This gene encodes a member of the zinc finger family of proteins. This gene shows decreased expression in cumulus cells derived from patients undergoing controlled ovarian stimulation. This gene is present in a gene cluster with several related zinc finger genes in the pericentromeric region of chromosome 10. Pseudogenes have been identified on chromosomes 7 and 10. Alternative splicing results in multiple transcript variants.

Source: NCBI Gene 7582 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 132 total
  • MANE Select transcript: NM_006955

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:13097
Approved symbolZNF33B
Namezinc finger protein 33B
Location10q11.21
Locus typegene with protein product
StatusApproved
AliasesKOX31, KOX2
Ensembl geneENSG00000196693
Ensembl biotypeprotein_coding
OMIM194522
Entrez7582

Gene structure

Transcript identifiers

Ensembl transcripts: 13 — 10 protein_coding, 2 retained_intron, 1 protein_coding_CDS_not_defined

ENST00000359467, ENST00000462075, ENST00000465206, ENST00000476796, ENST00000486187, ENST00000486614, ENST00000493285, ENST00000613419, ENST00000876414, ENST00000876415, ENST00000876416, ENST00000876417, ENST00000929479

RefSeq mRNA: 8 — MANE Select: NM_006955 NM_001305033, NM_001305035, NM_001305036, NM_001305037, NM_001305038, NM_001305039, NM_001305040, NM_006955

CCDS: CCDS7198

Canonical transcript exons

ENST00000359467 — 5 exons

ExonStartEnd
ENSE000014264264263847442638570
ENSE000034711754263229542632439
ENSE000036305534263692042636972
ENSE000037894464263192942632024
ENSE000038460004258910942594699

Expression profiles

Bgee: expression breadth ubiquitous, 235 present calls, max score 94.53.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 8.3449 / max 162.6621, expressed in 1614 samples.

FANTOM5 promoters (6 alternative TSS)

Promoter IDTPM avgSamples expressed
1091514.15221346
1091503.02491273
1091520.8368432
2058250.218691
1091480.059414
1091490.053112

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
body of pancreasUBERON:000115094.53gold quality
cortical plateUBERON:000534393.84gold quality
pancreasUBERON:000126490.69gold quality
right uterine tubeUBERON:000130289.40gold quality
ganglionic eminenceUBERON:000402389.28gold quality
left ovaryUBERON:000211987.81gold quality
islet of LangerhansUBERON:000000687.45gold quality
buccal mucosa cellCL:000233686.48gold quality
cerebellar hemisphereUBERON:000224586.45gold quality
germinal epithelium of ovaryUBERON:000130486.30gold quality
cerebellar cortexUBERON:000212986.26gold quality
minor salivary glandUBERON:000183086.19gold quality
calcaneal tendonUBERON:000370185.97gold quality
right hemisphere of cerebellumUBERON:001489085.76gold quality
saliva-secreting glandUBERON:000104485.74gold quality
ovaryUBERON:000099285.25gold quality
parotid glandUBERON:000183185.23gold quality
ventricular zoneUBERON:000305385.21gold quality
right ovaryUBERON:000211885.14gold quality
adrenal tissueUBERON:001830385.13gold quality
rectumUBERON:000105284.78gold quality
body of stomachUBERON:000116183.97gold quality
left lobe of thyroid glandUBERON:000112083.89gold quality
metanephros cortexUBERON:001053383.84gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047383.68gold quality
cerebellumUBERON:000203783.54gold quality
thyroid glandUBERON:000204683.54gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099183.51gold quality
right lobe of thyroid glandUBERON:000111983.49gold quality
mouth mucosaUBERON:000372983.24gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 4.

ExperimentMarker?Max mean expression
E-MTAB-8498yes854.86
E-ANND-3yes15.54
E-MTAB-6678yes10.63
E-MTAB-9801yes6.84

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): STAT1

miRNA regulators (miRDB)

119 targeting ZNF33B, 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-126-5P100.0072.713180
HSA-MIR-4795-3P100.0074.624024
HSA-MIR-8485100.0077.574731
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-4262100.0073.263931
HSA-MIR-548P99.9872.253784
HSA-MIR-477599.9875.006394
HSA-MIR-480399.9871.993117
HSA-MIR-548N99.9871.944170
HSA-MIR-548AJ-3P99.9673.385345
HSA-MIR-548X-3P99.9673.385345
HSA-MIR-590-3P99.9674.346478
HSA-MIR-493-5P99.9672.472382
HSA-MIR-548J-3P99.9472.614881
HSA-MIR-101-3P99.9475.032230
HSA-MIR-548AE-3P99.9372.664867
HSA-MIR-548AH-3P99.9372.544872
HSA-MIR-548AM-3P99.9372.544872
HSA-MIR-548AQ-3P99.9372.664867
HSA-MIR-3682-5P99.9367.971163
HSA-MIR-10527-5P99.9172.283754
HSA-MIR-368699.9070.532432
HSA-MIR-153-5P99.8973.866317
HSA-MIR-579-3P99.8671.663628
HSA-MIR-664B-3P99.8471.653590
HSA-MIR-469899.8471.414303
HSA-MIR-442099.8270.081624
HSA-MIR-181B-2-3P99.8170.061646
HSA-MIR-181B-3P99.8170.061646
HSA-MIR-374C-5P99.8072.062910

Literature-anchored findings (GeneRIF, showing 1)

  • Zinc finger protein 33B demonstrates sex interaction with atopy-related markers in childhood asthma. (PMID:35953101)

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 33BQ06732 (reviewed: Q06732)

Alternative names: Zinc finger protein 11B, Zinc finger protein KOX2

All UniProt accessions (5): Q06732, A0A087WVA3, A0A087WXF4, A0A087WXT3, A0A087X1D4

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.

RefSeq proteins (8): NP_001291962, NP_001291964, NP_001291965, NP_001291966, NP_001291967, NP_001291968, NP_001291969, NP_008886* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily
IPR050826Krueppel_C2H2_ZnFingerFamily

Pfam: PF00096, PF01352

UniProt features (27 total): zinc finger region 16, cross-link 5, sequence variant 2, sequence conflict 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q06732-F165.800.10

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (5): 181, 238, 313, 677, 733

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 82 (showing top): MORF_MSH3, MORF_BRCA1, LINDGREN_BLADDER_CANCER_CLUSTER_3_DN, MORF_RAD51L3, MORF_ATF2, MORF_PPP2R5B, KRIGE_RESPONSE_TO_TOSEDOSTAT_24HR_UP, MORF_MYL3, GAZDA_DIAMOND_BLACKFAN_ANEMIA_ERYTHROID_DN, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, MORF_IL16, MORF_DMPK, MORF_ERCC4, MORF_TFDP2, GOBP_NEGATIVE_REGULATION_OF_TRANSCRIPTION_BY_RNA_POLYMERASE_II

GO Biological Process (4): regulation of transcription by RNA polymerase II (GO:0006357), regulation of DNA-templated transcription (GO:0006355), regulation of macromolecule metabolic process (GO:0060255), regulation of primary metabolic process (GO:0080090)

GO Molecular Function (5): 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)

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 metabolic process2
regulation of DNA-templated transcription1
transcription by RNA polymerase II1
DNA-templated transcription1
regulation of gene expression1
regulation of RNA biosynthetic process1
macromolecule metabolic process1
primary metabolic process1
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

306 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF33BLHFPL7Q6ICI0587
ZNF33BLRRIQ3A6PVS8399
ZNF33BCCDC60Q8IWA6390
ZNF33BPPP2R5CQ13362375
ZNF33BVMA22Q96NT0372
ZNF33BHES7Q9BYE0372
ZNF33BKRTAP1-5Q9BYS1370
ZNF33BEVX1P49640321
ZNF33BMALRD1Q5VYJ5320
ZNF33BFNBP4Q8N3X1312
ZNF33BSLX4IPQ5VYV7305
ZNF33BFPGTO14772305
ZNF33BCHRM3P20309304
ZNF33BKRTAP1-1Q07627274
ZNF33BV9GXZ4V9GXZ4263

IntAct

13 interactions, top by confidence:

ABTypeScore
MAGEA12ZNF33Bpsi-mi:“MI:0915”(physical association)0.560
ZNF33BMAGEA12psi-mi:“MI:0915”(physical association)0.560
CBX6IGF2BP3psi-mi:“MI:0914”(association)0.530
TRIM28ZNF320psi-mi:“MI:0914”(association)0.530
ZNF33BHap1psi-mi:“MI:0915”(physical association)0.370
ZNF33BZHX1psi-mi:“MI:0915”(physical association)0.370
TRIM28ZNF320psi-mi:“MI:0914”(association)0.350
FMR1ZNF33Bpsi-mi:“MI:0915”(physical association)0.000
ZNF33BHAP1psi-mi:“MI:0915”(physical association)0.000

BioGRID (8): ZNF33B (Two-hybrid), ZNF33B (Affinity Capture-MS), ZNF33B (Affinity Capture-RNA), ZNF33B (Affinity Capture-MS), ZNF33B (Affinity Capture-MS), ZNF33B (Affinity Capture-MS), HAP1 (Two-hybrid), ZHX1 (Two-hybrid)

ESM2 similar proteins: A2VDP4, A6NHJ4, O94892, P0CJ79, P17014, P17021, P17025, P17032, P17035, P18733, P51508, P51814, Q06730, Q06732, Q09FC8, Q0VGE8, Q14586, Q32M78, Q3MIS6, Q5JVG2, Q5R4K8, Q5R9S5, Q5RBQ3, Q5RCJ2, Q5RER9, Q5TYW1, Q5VIY5, Q6P560, Q6PDB4, Q6ZMW2, Q6ZN06, Q6ZNA1, Q76KX8, Q7L2R6, Q86Y25, Q8N184, Q8N823, Q8N883, Q8N8J6, Q8NEP9

Diamond homologs: A0A1W2PQL4, A0JNB1, A0JPL0, A6NK53, A6QLU5, A6QPT6, A7MBI1, A8MT65, A8MUV8, A8MWA4, B2RXC5, B4DU55, B4DX44, E9PYI1, O14628, O75346, P0CH99, P0CI00, P17014, P17030, P17032, P17098, P51786, P85977, Q02386, Q06730, Q06732, Q0VAW7, Q12901, Q13360, Q14586, Q14588, Q14590, Q16587, Q2M3X9, Q2VY69, Q32M78, Q3ZCX4, Q49AA0, Q4R6J4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance124
Likely benign4
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

1798 predictions. Top by Δscore:

VariantEffectΔscore
10:42632294:CCCA:Cdonor_gain1.0000
10:42632297:A:ACdonor_gain1.0000
10:42632298:C:CCdonor_gain1.0000
10:42633253:A:ACdonor_gain1.0000
10:42633254:C:CCdonor_gain1.0000
10:42636970:CAG:Cacceptor_gain1.0000
10:42636978:T:Cacceptor_gain1.0000
10:42636978:T:TCacceptor_gain1.0000
10:42638468:GCTTA:Gdonor_loss1.0000
10:42638469:CTTAC:Cdonor_loss1.0000
10:42638471:TA:Tdonor_loss1.0000
10:42638472:A:ACdonor_gain1.0000
10:42638472:A:ATdonor_loss1.0000
10:42638473:C:CCdonor_gain1.0000
10:42638473:CCT:Cdonor_gain1.0000
10:42638473:CCTCA:Cdonor_gain1.0000
10:42594697:CTT:Cacceptor_gain0.9900
10:42631924:CCCA:Cdonor_loss0.9900
10:42631926:CAC:Cdonor_loss0.9900
10:42631927:A:ATdonor_loss0.9900
10:42631928:CC:Cdonor_loss0.9900
10:42631955:T:TAdonor_gain0.9900
10:42632021:TACC:Tacceptor_gain0.9900
10:42632023:CC:Cacceptor_gain0.9900
10:42632024:CC:Cacceptor_gain0.9900
10:42632850:T:TAdonor_gain0.9900
10:42633241:TGGA:Tdonor_gain0.9900
10:42636915:CTTA:Cdonor_loss0.9900
10:42636916:TTAC:Tdonor_loss0.9900
10:42636917:TACCT:Tdonor_loss0.9900

AlphaMissense

5227 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:42593600:G:CF450L0.999
10:42593600:G:TF450L0.999
10:42593602:A:GF450L0.999
10:42592844:G:CF702L0.998
10:42592844:G:TF702L0.998
10:42592846:A:GF702L0.998
10:42593096:G:CF618L0.998
10:42593096:G:TF618L0.998
10:42593098:A:GF618L0.998
10:42593331:A:GL540P0.998
10:42593432:G:CF506L0.998
10:42593432:G:TF506L0.998
10:42593434:A:GF506L0.998
10:42593499:A:GL484P0.998
10:42593516:A:CF478L0.998
10:42593516:A:TF478L0.998
10:42593518:A:GF478L0.998
10:42593583:A:GL456P0.998
10:42593768:A:CF394L0.998
10:42593768:A:TF394L0.998
10:42593770:A:GF394L0.998
10:42593079:A:GL624P0.997
10:42593163:A:GL596P0.997
10:42593247:A:GL568P0.997
10:42593348:G:CF534L0.997
10:42593348:G:TF534L0.997
10:42593350:A:GF534L0.997
10:42593667:A:GL428P0.997
10:42593679:T:GQ424P0.997
10:42593684:A:CF422L0.997

dbSNP variants (sampled 300 via entrez): RS1000003382 (10:42629870 T>C), RS1000007341 (10:42588827 T>C), RS1000059373 (10:42623481 T>C), RS1000137349 (10:42620689 G>A), RS1000147841 (10:42589119 A>G), RS1000257224 (10:42624060 G>A), RS1000266161 (10:42617453 T>C), RS1000284200 (10:42639657 G>A), RS1000394011 (10:42594865 G>C), RS1000454819 (10:42625049 T>C), RS1000509670 (10:42584543 CAG>C), RS1000550985 (10:42630176 A>AT), RS1000563730 (10:42579834 C>T), RS1000577188 (10:42583434 C>A), RS1000740886 (10:42619304 C>T)

Disease associations

OMIM: gene MIM:194522 | 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
GCST004025_10Systemic juvenile idiopathic arthritis1.000000e-06
GCST007272_23Pulse pressure3.000000e-44

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0005763pulse pressure measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

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

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, affects cotreatment, increases abundance, increases expression3
Resveratrolaffects cotreatment, increases expression, decreases expression2
Tobacco Smoke Pollutiondecreases expression2
Valproic Aciddecreases expression2
Cyclosporineincreases expression2
Cadmium Chloridedecreases expression, increases expression2
aristolochic acid Idecreases expression1
dicrotophosdecreases expression1
methylmercuric chloridedecreases expression1
triphenyl phosphateaffects expression1
trichostatin Aaffects expression1
sulforaphanedecreases expression1
butyraldehydedecreases expression1
manganese chlorideincreases abundance, increases expression1
coumarindecreases phosphorylation1
abrinedecreases expression1
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidineincreases expression, increases response to substance1
jinfukangaffects cotreatment, increases expression1
NSC 689534affects binding, increases expression1
Sunitinibincreases expression1
Arsenic Trioxidedecreases expression1
Air Pollutantsdecreases expression, increases abundance1
Ethanoldecreases expression1
Arsenicincreases expression, affects cotreatment, increases abundance1
Cisplatinincreases expression, affects cotreatment1
Coaldecreases expression, increases abundance1
Copperaffects binding, increases expression1
Manganeseincreases abundance, increases expression1
Methyl Methanesulfonateincreases expression1
Nickeldecreases expression1

Clinical trials (associated diseases)

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