PBOV1

gene
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Also known as UC28UROC28

Summary

PBOV1 (prostate and breast cancer overexpressed 1, HGNC:21079) is a protein-coding gene on chromosome 6q23.3, encoding Prostate and breast cancer overexpressed gene 1 protein (Q9GZY1).

This intronless gene encodes a protein of unknown function. Its expression is up-regulated in some types of cancer, including prostate, breast, and bladder cancer.

Source: NCBI Gene 59351 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_021635

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:21079
Approved symbolPBOV1
Nameprostate and breast cancer overexpressed 1
Location6q23.3
Locus typegene with protein product
StatusApproved
AliasesUC28, UROC28
Ensembl geneENSG00000254440
Ensembl biotypeprotein_coding
OMIM605669
Entrez59351

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000527246

RefSeq mRNA: 1 — MANE Select: NM_021635 NM_021635

CCDS: CCDS5190

Canonical transcript exons

ENST00000527246 — 1 exons

ExonStartEnd
ENSE00002142146138215986138218491

Expression profiles

Bgee: expression breadth broad, 14 present calls, max score 63.03.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039763.03silver quality
epithelium of nasopharynxUBERON:000195162.12gold quality
corpus callosumUBERON:000233658.44gold quality
bone marrow cellCL:000209258.36gold quality
buccal mucosa cellCL:000233655.71gold quality
oocyteCL:000002355.30gold quality
spermCL:000001954.04gold quality
nasal cavity epitheliumUBERON:000538452.74gold quality
lower lobe of lungUBERON:000894952.65silver quality
heart right ventricleUBERON:000208052.17gold quality
metanephros cortexUBERON:001053351.25gold quality
tonsilUBERON:000237248.19gold quality
metanephrosUBERON:000008147.97gold quality
oviduct epitheliumUBERON:000480447.93silver quality
lateral nuclear group of thalamusUBERON:000273647.65gold quality
tendon of biceps brachiiUBERON:000818846.84gold quality
bone marrowUBERON:000237145.54gold quality
cardia of stomachUBERON:000116245.37gold quality
upper leg skinUBERON:000426245.04silver quality
substantia nigra pars reticulataUBERON:000196644.62gold quality
adult organismUBERON:000702343.72gold quality
skeletal muscle tissueUBERON:000113443.65gold quality
gingivaUBERON:000182843.56gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality
tendonUBERON:000004343.17gold quality
ventral tegmental areaUBERON:000269143.00gold quality
gingival epitheliumUBERON:000194942.58gold quality
secondary oocyteCL:000065542.57gold quality
calcaneal tendonUBERON:000370142.47gold quality
germinal epithelium of ovaryUBERON:000130441.90gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.44

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

73 targeting PBOV1, 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-4668-3P100.0068.742635
HSA-MIR-1277-5P100.0073.955056
HSA-MIR-568899.9673.234504
HSA-MIR-495-3P99.9672.814197
HSA-MIR-545-3P99.9570.742783
HSA-MIR-335-3P99.9373.364958
HSA-MIR-454-3P99.9174.011925
HSA-MIR-130599.9171.433443
HSA-MIR-130A-3P99.9073.311861
HSA-MIR-130B-3P99.9073.271850
HSA-MIR-301A-3P99.9073.151839
HSA-MIR-301B-3P99.9073.191836
HSA-MIR-366699.9073.241833
HSA-MIR-429599.9073.111838
HSA-MIR-627-3P99.9071.423316
HSA-MIR-4731-5P99.8967.232537
HSA-MIR-5010-3P99.8370.602357
HSA-MIR-6739-5P99.8067.872806
HSA-MIR-129999.7771.242389
HSA-MIR-6733-5P99.7467.942759
HSA-MIR-132-3P99.7370.561424
HSA-MIR-212-3P99.7370.651424
HSA-MIR-33A-3P99.7070.273362
HSA-MIR-472999.6972.184233
HSA-MIR-320299.6667.702737
HSA-MIR-58699.6570.402051
HSA-MIR-6848-3P99.6466.49885
HSA-MIR-885-5P99.5968.59879
HSA-MIR-211399.5871.221521
HSA-MIR-467299.5071.582893

Literature-anchored findings (GeneRIF, showing 6)

  • UROC28 mRNA expression was greater in breast cancers than in noncancerous tissues (p < 0.0001), as was ERBB2 mRNA. (PMID:12553037)
  • Approximately half of the prostate tumors displayed increased copy numbers of the BMP2, BMP5, BMP7, and UC28 gene loci, which may account for their abnormal gene expression patterns in neoplastic prostate tissue. (PMID:17656261)
  • Data indicate that analysis of public microarray data suggests that PBOV1 activation in tumors could be dependent on the Hedgehog signaling pathway. (PMID:23418531)
  • Study shows that patients with high PBOV1 expression had longer overall survival; patients with low PBOV1 expression had shorter survival suggesting that PBOV1 may play an important role in suppressing ovarian cancer proliferation and carcinogenesis. (PMID:26549570)
  • Overexpression of PBOV1 in THP-1 cells resulted in cell cycle G1 arrest, differentiation into macrophages, a marked increase in IL-10 and CXCL10 mRNA levels, and upregulation of the costimulatory molecules. (PMID:30231487)
  • FBXL19AS1 promotes the progression of nasopharyngeal carcinoma by acting as a competing endogenous RNA to sponge miR431 and upregulate PBOV1. (PMID:34278444)

Cross-species orthologs

0 orthologs

Protein

Protein identifiers

Prostate and breast cancer overexpressed gene 1 proteinQ9GZY1 (reviewed: Q9GZY1)

Alternative names: Protein UROC28

All UniProt accessions (1): Q9GZY1

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Cytoplasm. Nucleus.

Tissue specificity. Expressed in colon, prostate, small intestine, testis and spleen, with lower expression in thymus, ovary, and peripheral blood leukocytes. Up-regulated expression in prostate, breast, and bladder cancer, but not in lung and colon cancer.

RefSeq proteins (1): NP_067648* (*=MANE)

Domains & families (InterPro)

UniProt features (2 total): chain 1, sequence variant 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9GZY1-F151.830.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 24 (showing top): ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, TAATTA_CHX10_01, chr6q23, CHICAS_RB1_TARGETS_CONFLUENT, KRIEG_HYPOXIA_NOT_VIA_KDM3A, NOTCH_DN.V1_DN, MIR5688, MIR495_3P, MIR4291, MIR5010_3P, MIR3978, MIR212_3P, MIR132_3P, MIR504_3P, MIR885_5P

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (5): nucleoplasm (GO:0005654), cytosol (GO:0005829), centriolar satellite (GO:0034451), nucleus (GO:0005634), cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure4
nuclear lumen1
cytoplasm1
centrosome1
intracellular membrane-bounded organelle1
intracellular anatomical structure1

Protein interactions and networks

STRING

36 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
PBOV1ESCO1Q5FWF5222
PBOV1BMP5P22003222
PBOV1ESCO2Q56NI9221
PBOV1HHLA1C9JL84201
PBOV1CEBPBP17676200
PBOV1FOXA1P55317181
PBOV1ISM2Q6H9L7176
PBOV1EYA4O95677174
PBOV1AFF4Q9UHB7167
PBOV1HNRNPLP14866163
PBOV1CT47A11Q5JQC4161
PBOV1TMC6Q7Z403161
PBOV1ATOH7Q8N100160
PBOV1SOCS7O14512159
PBOV1HNRNPUQ00839159

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A023PXH2, A8MS09, B0L3A2, B6HUQ5, G2TRK6, G2TRL6, G2TRL8, G3V211, O13536, O14599, O30141, P03935, P05678, P0CE96, P0CE97, P0CE98, P19282, P38296, P38476, P39725, P40211, P53132, P53175, P53229, P53342, P75202, P92561, Q02918, Q03864, Q04434, Q07746, Q0Q027, Q10300, Q12174, Q12225, Q12327, Q3E7B9, Q54UZ5, Q65962, Q6B108

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance1
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

63 predictions. Top by Δscore:

VariantEffectΔscore
6:138218300:G:GTdonor_gain0.8500
6:138216617:T:Gacceptor_gain0.7900
6:138216616:T:TGacceptor_gain0.7400
6:138218300:G:Tacceptor_gain0.6800
6:138218401:CTA:Cdonor_gain0.5600
6:138216752:T:Gdonor_gain0.5400
6:138218400:A:ACdonor_gain0.5300
6:138218401:C:CCdonor_gain0.5300
6:138218397:T:Cdonor_gain0.4600
6:138216523:AT:Adonor_gain0.4200
6:138218469:GCCAC:Gdonor_loss0.4100
6:138218470:CCA:Cdonor_loss0.4100
6:138218471:CACCT:Cdonor_loss0.4100
6:138218472:A:Tdonor_loss0.4100
6:138218473:C:CCdonor_loss0.4100
6:138218474:C:Gdonor_loss0.4000
6:138216861:G:Tdonor_gain0.3900
6:138218291:T:TAdonor_gain0.3900
6:138218292:A:AAdonor_gain0.3900
6:138217399:CATAG:Cacceptor_gain0.3700
6:138218486:AAGGT:Adonor_gain0.3600
6:138217399:C:Tacceptor_gain0.3500
6:138218401:C:CTdonor_gain0.3500
6:138218402:T:TTdonor_gain0.3500
6:138218475:T:Adonor_loss0.3400
6:138218475:T:TAdonor_gain0.3400
6:138218402:T:Cdonor_gain0.3300
6:138218403:A:ACdonor_gain0.3300
6:138218404:C:CCdonor_gain0.3300
6:138218456:TA:Tdonor_gain0.3300

AlphaMissense

877 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
6:138218237:A:CF53L0.885
6:138218237:A:TF53L0.885
6:138218239:A:GF53L0.885
6:138218300:G:CF32L0.806
6:138218300:G:TF32L0.806
6:138218302:A:GF32L0.806
6:138218192:G:CF68L0.788
6:138218192:G:TF68L0.788
6:138218194:A:GF68L0.788
6:138218028:A:GL123P0.758
6:138218384:G:CF4L0.754
6:138218384:G:TF4L0.754
6:138218386:A:GF4L0.754
6:138218145:A:GL84S0.751
6:138218251:A:GC49R0.746
6:138218032:A:GC122R0.716
6:138218058:A:GL113S0.699
6:138218238:A:GF53S0.684
6:138218252:G:CF48L0.664
6:138218252:G:TF48L0.664
6:138218254:A:GF48L0.664
6:138218249:G:CC49W0.662
6:138218157:A:CI80S0.640
6:138218238:A:CF53C0.640
6:138218324:T:AK24N0.628
6:138218324:T:GK24N0.628
6:138218157:A:TI80N0.623
6:138218037:T:AE120V0.616
6:138218327:T:AR23S0.616
6:138218327:T:GR23S0.616

dbSNP variants (sampled 300 via entrez): RS1001295795 (6:138217649 G>A), RS1002749961 (6:138215896 G>A), RS1004831125 (6:138219654 G>T), RS1004881953 (6:138219308 G>A), RS1005700290 (6:138216558 T>C), RS1006538098 (6:138215667 A>C), RS1008180379 (6:138216781 A>G), RS1008213204 (6:138217132 A>C), RS1008548320 (6:138218443 T>A,C), RS1009048883 (6:138219984 T>A), RS1009122294 (6:138220181 T>C), RS1009812438 (6:138219952 G>A), RS1010254073 (6:138219620 T>C), RS1011739316 (6:138219982 AT>A,ATT), RS1012183567 (6:138220201 C>A,T)

Disease associations

OMIM: gene MIM:605669 | 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

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
CGP 52608affects binding, increases reaction1
Benzo(a)pyreneincreases methylation1
Estradioldecreases expression1

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.