ZNF324B

gene
On this page

Also known as FLJ45850

Summary

ZNF324B (zinc finger protein 324B, HGNC:33107) is a protein-coding gene on chromosome 19q13.43, encoding Zinc finger protein 324B (Q6AW86). 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 388569 — RefSeq curated summary.

At a glance

  • GWAS associations: 1
  • Clinical variants (ClinVar): 100 total
  • MANE Select transcript: NM_207395

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:33107
Approved symbolZNF324B
Namezinc finger protein 324B
Location19q13.43
Locus typegene with protein product
StatusApproved
AliasesFLJ45850
Ensembl geneENSG00000249471
Ensembl biotypeprotein_coding
Entrez388569

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 19 protein_coding

ENST00000336614, ENST00000545523, ENST00000594214, ENST00000598244, ENST00000599193, ENST00000599194, ENST00000869294, ENST00000869295, ENST00000869296, ENST00000869297, ENST00000869298, ENST00000928892, ENST00000928893, ENST00000963232, ENST00000963233, ENST00000963234, ENST00000963235, ENST00000963236, ENST00000963237

RefSeq mRNA: 1 — MANE Select: NM_207395 NM_207395

CCDS: CCDS33138

Canonical transcript exons

ENST00000336614 — 4 exons

ExonStartEnd
ENSE000014694745845518358457833
ENSE000014694765845162258451704
ENSE000036774965845369658453822
ENSE000037896315845422858454344

Expression profiles

Bgee: expression breadth ubiquitous, 163 present calls, max score 81.91.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 4.2841 / max 48.3036, expressed in 1620 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1778464.28411620

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.91silver quality
cortical plateUBERON:000534376.71gold quality
sural nerveUBERON:001548876.30gold quality
stromal cell of endometriumCL:000225574.42gold quality
ventricular zoneUBERON:000305373.07gold quality
prefrontal cortexUBERON:000045172.77gold quality
pancreatic ductal cellCL:000207972.43silver quality
ganglionic eminenceUBERON:000402372.13gold quality
gastrocnemiusUBERON:000138871.72gold quality
granulocyteCL:000009471.58gold quality
muscle of legUBERON:000138371.12gold quality
cervix squamous epitheliumUBERON:000692271.06gold quality
right uterine tubeUBERON:000130270.72gold quality
skin of legUBERON:000151170.68gold quality
endocervixUBERON:000045870.48gold quality
islet of LangerhansUBERON:000000670.42gold quality
skin of abdomenUBERON:000141670.16gold quality
leukocyteCL:000073870.15gold quality
right ovaryUBERON:000211870.02gold quality
monocyteCL:000057670.01gold quality
mononuclear cellCL:000084269.83gold quality
body of pancreasUBERON:000115069.70gold quality
lower esophagus muscularis layerUBERON:003583369.67gold quality
lower esophagusUBERON:001347369.62gold quality
ectocervixUBERON:001224969.41gold quality
pancreasUBERON:000126469.30gold quality
mucosa of stomachUBERON:000119969.24gold quality
esophagusUBERON:000104369.22gold quality
esophagus mucosaUBERON:000246969.15gold quality
body of stomachUBERON:000116169.13gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.55

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

33 targeting ZNF324B, 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-3689D100.0066.141181
HSA-MIR-6851-5P100.0065.631294
HSA-MIR-6798-5P100.0065.77699
HSA-MIR-5193100.0067.261744
HSA-MIR-453499.9966.581907
HSA-MIR-3667-3P99.9967.171636
HSA-MIR-3605-5P99.9667.12932
HSA-MIR-426799.9666.532368
HSA-MIR-449399.9066.48977
HSA-MIR-444799.8567.812900
HSA-MIR-7110-5P99.8067.841712
HSA-MIR-6842-5P99.8067.541587
HSA-MIR-320299.6667.702737
HSA-MIR-4753-5P99.5468.511356
HSA-MIR-136-5P99.5067.261153
HSA-MIR-239299.4367.50708
HSA-MIR-807799.1766.67862
HSA-MIR-4695-5P99.0664.871151
HSA-MIR-589-5P98.7266.96927
HSA-MIR-1227-5P98.6565.321549
HSA-MIR-6852-3P98.5467.601468
HSA-MIR-7114-5P98.5167.871349
HSA-MIR-4684-3P98.2469.911075
HSA-MIR-4717-5P98.1967.97894
HSA-MIR-451898.1266.821030
HSA-MIR-432-5P98.0068.13989
HSA-MIR-6502-3P97.8665.43569
HSA-MIR-3664-3P97.8567.621452
HSA-MIR-1266-5P97.7166.921052
HSA-MIR-6859-3P97.2664.69428

Cross-species orthologs

6 orthologs

OrganismSymbolGene ID
danio_rerio42sp43ENSDARG00000104170
mus_musculusZfp324ENSMUSG00000004500
rattus_norvegicusZfp324ENSRNOG00000027436
drosophila_melanogasterdwgFBGN0000520
drosophila_melanogasterCG6654FBGN0038301
caenorhabditis_elegansWBGENE00003933

Paralogs (6): ZNF324 (ENSG00000083812), ZBTB47 (ENSG00000114853), GTF3A (ENSG00000122034), ZUP1 (ENSG00000153975), ZNF513 (ENSG00000163795), ZNF652 (ENSG00000198740)

Protein

Protein identifiers

Zinc finger protein 324BQ6AW86 (reviewed: Q6AW86)

All UniProt accessions (5): Q6AW86, M0R090, M0R0B1, M0R1X9, M0R3B5

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?
Q6AW86-11yes
Q6AW86-22

RefSeq proteins (1): NP_997278* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001909KRABDomain
IPR013087Znf_C2H2_typeDomain
IPR036051KRAB_dom_sfHomologous_superfamily
IPR036236Znf_C2H2_sfHomologous_superfamily

Pfam: PF00096, PF01352

UniProt features (19 total): zinc finger region 9, region of interest 2, sequence conflict 2, chain 1, domain 1, compositionally biased region 1, cross-link 1, splice variant 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6AW86-F164.800.35

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 (1): 214

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-212436Generic Transcription Pathway

MSigDB gene sets: 36 (showing top): PARENT_MTOR_SIGNALING_UP, MOREAUX_MULTIPLE_MYELOMA_BY_TACI_UP, GOMF_SEQUENCE_SPECIFIC_DNA_BINDING, SMAD_Q6, TORCHIA_TARGETS_OF_EWSR1_FLI1_FUSION_UP, ATF2_S_UP.V1_UP, ATF2_UP.V1_UP, IL21_UP.V1_DN, GOMF_TRANSCRIPTION_REGULATOR_ACTIVITY, CEBPZ_TARGET_GENES, PCGF1_TARGET_GENES, ZNF669_TARGET_GENES, ZNF768_TARGET_GENES, MIR3202, GSE10240_IL17_VS_IL17_AND_IL22_STIM_PRIMARY_BRONCHIAL_EPITHELIAL_CELLS_UP

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

GO Molecular Function (5): 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), 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
cation binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

574 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
ZNF324BEID2Q8N6I1635
ZNF324BRABEP2Q9H5N1633
ZNF324BYIPF4Q9BSR8540
ZNF324BFRMD5Q7Z6J6480
ZNF324BCCDC127Q96BQ5445
ZNF324BASB7Q9H672414
ZNF324BSUPT7LO94864409
ZNF324BCAPN10Q9HC96403
ZNF324BTMC8Q8IU68400
ZNF324BPCMT1P22061391
ZNF324BRPS7P23821388
ZNF324BCNOT10Q9H9A5362
ZNF324BCOMMD5Q9GZQ3343
ZNF324BTADA2BQ86TJ2329
ZNF324BGJD3Q8N144329

IntAct

12 interactions, top by confidence:

ABTypeScore
ZNF324BZNF316psi-mi:“MI:0914”(association)0.530
ZNF324BZNF324psi-mi:“MI:0914”(association)0.530
KISS1RERLIN1psi-mi:“MI:0915”(physical association)0.400
RGS3ZNF646psi-mi:“MI:0914”(association)0.350
CBX5ZNF568psi-mi:“MI:0914”(association)0.350
NOTCH2ZNF320psi-mi:“MI:0914”(association)0.350
LTBP2ZNF320psi-mi:“MI:0914”(association)0.350
LRP3TMEM131Lpsi-mi:“MI:0914”(association)0.350

BioGRID (150): ZNF324 (Affinity Capture-MS), SPIN3 (Affinity Capture-MS), ACTA1 (Affinity Capture-MS), ZNF324B (Affinity Capture-MS), RBAK (Affinity Capture-MS), TRIM24 (Affinity Capture-MS), SPIN1 (Affinity Capture-MS), NGRN (Affinity Capture-MS), HELZ2 (Affinity Capture-MS), ZNF184 (Affinity Capture-MS), ZNF460 (Affinity Capture-MS), ZNF746 (Affinity Capture-MS), ZNF316 (Affinity Capture-MS), TOPORS (Affinity Capture-MS), RPF1 (Affinity Capture-MS)

ESM2 similar proteins: A3KN32, A6NM28, A8K8V0, E9PYI1, O75467, O95201, P10072, P10075, P10078, P10754, P28698, P30373, P52736, Q0VCC5, Q14929, Q16587, Q17QR7, Q29RZ4, Q3KNW1, Q3TDE8, Q3US17, Q58DK7, Q5RJR4, Q5T619, Q5TEC3, Q5U4E2, Q62396, Q68H95, Q6AW86, Q6PGE4, Q6ZMY9, Q7Z398, Q7Z7K2, Q8BI73, Q8BIF9, Q8BIQ3, Q8BKK5, Q8JZL0, Q8N393, Q8R0T2

Diamond homologs: A0JPL0, A2A761, A3KN32, A3KN36, A6NFI3, A6NM28, A6QLU5, A6QPT6, A7MBI1, A8MTY0, B2RXC5, B4DU55, E9PYI1, O14978, O60765, O75467, O75820, O95780, P0C7X2, P0DKX0, P0DPD5, P10072, P15622, P16374, P17014, P17023, P17032, P17098, P51523, P51786, P52738, P52742, Q02975, Q06732, Q08DG8, Q08ER8, Q0VCB0, Q14590, Q14929, Q29RZ4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance87
Likely benign12
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1216 predictions. Top by Δscore:

VariantEffectΔscore
19:58453685:T:TAacceptor_gain1.0000
19:58453688:T:Aacceptor_gain1.0000
19:58453691:TTTAG:Tacceptor_loss1.0000
19:58453694:A:AGacceptor_gain1.0000
19:58453694:AG:Aacceptor_gain1.0000
19:58453695:G:GAacceptor_gain1.0000
19:58453695:GG:Gacceptor_gain1.0000
19:58453695:GGA:Gacceptor_gain1.0000
19:58453695:GGAC:Gacceptor_gain1.0000
19:58453695:GGACC:Gacceptor_gain1.0000
19:58453818:ACTTG:Adonor_gain1.0000
19:58453819:CTTG:Cdonor_gain1.0000
19:58453823:G:GGdonor_gain1.0000
19:58453824:T:Gdonor_loss1.0000
19:58453828:GCCC:Gdonor_gain1.0000
19:58454223:CACA:Cacceptor_loss1.0000
19:58454225:CAGG:Cacceptor_loss1.0000
19:58454226:A:AGacceptor_gain1.0000
19:58454226:A:Tacceptor_loss1.0000
19:58454227:G:GGacceptor_gain1.0000
19:58454227:GGA:Gacceptor_gain1.0000
19:58454227:GGACT:Gacceptor_gain1.0000
19:58454252:T:TAacceptor_gain1.0000
19:58454345:G:GGdonor_gain1.0000
19:58454345:G:Tdonor_loss1.0000
19:58451655:G:GAdonor_gain0.9900
19:58451702:A:Tdonor_gain0.9900
19:58451754:G:GGdonor_gain0.9900
19:58451828:G:GTdonor_gain0.9900
19:58453820:TTG:Tdonor_gain0.9900

AlphaMissense

3552 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:58455824:T:CF294L0.999
19:58455826:C:AF294L0.999
19:58455826:C:GF294L0.999
19:58455908:T:CF322L0.999
19:58455910:C:AF322L0.999
19:58455910:C:GF322L0.999
19:58455992:T:CF350L0.999
19:58455994:C:AF350L0.999
19:58455994:C:GF350L0.999
19:58456076:T:CF378L0.999
19:58456078:C:AF378L0.999
19:58456078:C:GF378L0.999
19:58455740:T:CF266L0.998
19:58455742:C:AF266L0.998
19:58455742:C:GF266L0.998
19:58455759:T:CL272P0.998
19:58455769:C:AH275Q0.998
19:58455769:C:GH275Q0.998
19:58456160:T:CF406L0.998
19:58456162:C:AF406L0.998
19:58456162:C:GF406L0.998
19:58456244:T:CF434L0.998
19:58456246:T:AF434L0.998
19:58456246:T:GF434L0.998
19:58456328:T:CF462L0.998
19:58456330:C:AF462L0.998
19:58456330:C:GF462L0.998
19:58456412:T:CF490L0.998
19:58456414:C:AF490L0.998
19:58456414:C:GF490L0.998

dbSNP variants (sampled 300 via entrez): RS1000128585 (19:58418548 C>T), RS1000253189 (19:58420376 A>G), RS1000304254 (19:58435991 T>G), RS1000334350 (19:58419284 G>A,T), RS1000420382 (19:58452022 G>T), RS1000528968 (19:58458115 G>A), RS1000635398 (19:58447892 G>A), RS1000696123 (19:58446127 T>C,G), RS1000726993 (19:58446420 A>G), RS1000786057 (19:58438288 C>T), RS1000796266 (19:58442421 G>A,C,T), RS1000863909 (19:58441361 T>G), RS1000891652 (19:58429962 C>A,T), RS1000960032 (19:58425136 G>C), RS1000975710 (19:58425561 G>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

1 associations (top):

StudyTraitp-value
GCST004599_201Mean platelet volume1.000000e-10

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

12 total (human), top 12 by PubMed support.

ChemicalActions (top 5)PubMed papers
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
ferrous chloridedecreases expression1
di-n-butylphosphoric acidaffects expression1
Arsenicaffects methylation1
Benzo(a)pyrenedecreases methylation1
Calcitrioldecreases expression, affects cotreatment1
Estradiolincreases expression1
Smokedecreases expression1
Testosteroneaffects cotreatment, decreases expression1
Urethanedecreases expression1
Valproic Acidincreases methylation1

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.