PDRG1

gene
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Also known as dJ310O13.3

Summary

PDRG1 (p53 and DNA damage regulated 1, HGNC:16119) is a protein-coding gene on chromosome 20q11.21, encoding p53 and DNA damage-regulated protein 1 (Q9NUG6). May play a role in chaperone-mediated protein folding. It is a common-essential gene (DepMap: required in 99.8% of cancer cell lines).

Predicted to enable unfolded protein binding activity. Predicted to be involved in protein stabilization. Part of RPAP3/R2TP/prefoldin-like complex.

Source: NCBI Gene 81572 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 13 total
  • Cancer dependency (DepMap): dependent in 99.8% of screened cell lines (common-essential)
  • MANE Select transcript: NM_030815

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:16119
Approved symbolPDRG1
Namep53 and DNA damage regulated 1
Location20q11.21
Locus typegene with protein product
StatusApproved
AliasesdJ310O13.3
Ensembl geneENSG00000088356
Ensembl biotypeprotein_coding
OMIM610789
Entrez81572

Gene structure

Transcript identifiers

Ensembl transcripts: 6 — 6 protein_coding

ENST00000202017, ENST00000902322, ENST00000902323, ENST00000902324, ENST00000902325, ENST00000918734

RefSeq mRNA: 1 — MANE Select: NM_030815 NM_030815

CCDS: CCDS13194

Canonical transcript exons

ENST00000202017 — 5 exons

ExonStartEnd
ENSE000006611373194649631946576
ENSE000006611383194880831948882
ENSE000006611393195031231950387
ENSE000011095043194433731945889
ENSE000011557393195187531952046

Expression profiles

Bgee: expression breadth ubiquitous, 245 present calls, max score 92.24.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 20.1101 / max 185.4348, expressed in 1808 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
18688718.95391805
1868850.8152460
1868860.3409183

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207992.24silver quality
right testisUBERON:000453492.22gold quality
left testisUBERON:000453391.97gold quality
kidney epitheliumUBERON:000481991.68silver quality
testisUBERON:000047390.88gold quality
cerebellar vermisUBERON:000472089.43gold quality
dorsal root ganglionUBERON:000004489.36gold quality
cerebellar hemisphereUBERON:000224587.95gold quality
cerebellar cortexUBERON:000212987.92gold quality
right hemisphere of cerebellumUBERON:001489087.82gold quality
cardiac muscle of right atriumUBERON:000337987.60gold quality
cerebellumUBERON:000203787.47gold quality
oocyteCL:000002387.11gold quality
trigeminal ganglionUBERON:000167587.10gold quality
left ventricle myocardiumUBERON:000656686.91gold quality
deltoidUBERON:000147686.78silver quality
secondary oocyteCL:000065586.46gold quality
ileal mucosaUBERON:000033185.92gold quality
tibial nerveUBERON:000132385.53gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099185.28gold quality
C1 segment of cervical spinal cordUBERON:000646985.22gold quality
mucosa of transverse colonUBERON:000499185.15gold quality
quadriceps femorisUBERON:000137784.98silver quality
prefrontal cortexUBERON:000045184.80gold quality
spinal cordUBERON:000224084.78gold quality
granulocyteCL:000009484.68gold quality
gastrocnemiusUBERON:000138884.54gold quality
ponsUBERON:000098884.44gold quality
adult organismUBERON:000702384.38gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047384.18gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes8.26

Regulation

Is transcription factor: no

Upstream regulators (CollecTRI, top): POU2F1, TP53

miRNA regulators (miRDB)

44 targeting PDRG1, 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-4425100.0067.591049
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-454-3P99.9174.011925
HSA-MIR-498-3P99.9171.271114
HSA-MIR-106A-5P99.9073.942683
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-17-5P99.8973.832665
HSA-MIR-106B-5P99.8874.722795
HSA-MIR-20A-5P99.8874.762769
HSA-MIR-20B-5P99.8874.012621
HSA-MIR-519D-3P99.8873.972607
HSA-MIR-526B-3P99.8874.062587
HSA-MIR-93-5P99.8873.982606
HSA-MIR-519A-3P99.6771.671868
HSA-MIR-519B-3P99.6771.671868
HSA-MIR-519C-3P99.6771.671870
HSA-MIR-4690-5P99.6566.24813
HSA-MIR-330-3P99.4169.952521
HSA-MIR-4667-3P99.2665.451608
HSA-MIR-6510-5P99.1466.591081
HSA-MIR-4758-3P99.1263.96869
HSA-MIR-3619-5P99.0068.872308
HSA-MIR-214-3P98.7168.122128
HSA-MIR-76198.7168.072051
HSA-MIR-6761-5P98.7168.031504

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 99.8% of screened cell lines, common-essential.

Literature-anchored findings (GeneRIF, showing 8)

  • Cloning and characterization of a novel gene PDRG that is differentially regulated by p53 and ultraviolet radiation (PMID:14562055)
  • Is part of an RNA polymerase II-associated complex with possible chaperone activity. (PMID:19450687)
  • PDRG1 expression is increased in multiple human malignancies suggesting it to be a high-value novel tumor marker that could play a role in cancer development and/or progression. (PMID:21193842)
  • It was found that PDRG1 could promote radio-resistance that involved the ATM-p53 signaling pathway in lung cancer cells. (PMID:27610824)
  • Specific PDRG1 gene silencing may inhibit the growth and metastasis of gastric cancer cells through the activation of ATM/p53 pathway. (PMID:31383535)
  • PDRG1 association with the Wnt signaling pathway in esophageal cancer cells.PDRG1 may promote proliferation while inhibiting apoptosis and chemotherapy sensitivity in esophageal cancer cells. (PMID:31882431)
  • PDRG1 predicts a poor prognosis and facilitates the proliferation and metastasis of colorectal cancer. (PMID:34780783)
  • PDRG1 promotes the proliferation and migration of GBM cells by the MEK/ERK/CD44 pathway. (PMID:34812552)

Cross-species orthologs

5 orthologs

OrganismSymbolGene ID
danio_reriopdrg1ENSDARG00000045017
mus_musculusPdrg1ENSMUSG00000027472
rattus_norvegicusPdrg1ENSRNOG00000008845
drosophila_melanogasterPdrg1FBGN0033467
caenorhabditis_elegansWBGENE00045407

Protein

Protein identifiers

p53 and DNA damage-regulated protein 1Q9NUG6 (reviewed: Q9NUG6)

All UniProt accessions (2): Q9NUG6, A0A384NKN4

UniProt curated annotations — full annotation on UniProt →

Function. May play a role in chaperone-mediated protein folding.

Subunit / interactions. Component of the PAQosome complex which is responsible for the biogenesis of several protein complexes and which consists of R2TP complex members RUVBL1, RUVBL2, RPAP3 and PIH1D1, URI complex members PFDN2, PFDN6, PDRG1, UXT and URI1 as well as ASDURF, POLR2E and DNAAF10/WDR92.

Subcellular location. Cytoplasm.

Tissue specificity. Predominantly expressed in normal testis and exhibits reduced but detectable expression in other organs.

Induction. By UV irradiation and repressed by p53/TP53.

Similarity. Belongs to the prefoldin subunit beta family.

RefSeq proteins (1): NP_110442* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR002777PFD_beta-likeFamily
IPR030482PDRG1Family

Pfam: PF01920

UniProt features (1 total): chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9NUG6-F192.160.78

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 117 (showing top): RODRIGUES_THYROID_CARCINOMA_ANAPLASTIC_UP, LFA1_Q6, GRAESSMANN_APOPTOSIS_BY_DOXORUBICIN_UP, GRAESSMANN_RESPONSE_TO_MC_AND_DOXORUBICIN_UP, GOBP_PROTEIN_MATURATION, GROSS_HYPOXIA_VIA_ELK3_UP, GOBP_PROTEIN_STABILIZATION, GROSS_HYPOXIA_VIA_ELK3_ONLY_DN, GOBP_PROTEIN_FOLDING, GOBP_REGULATION_OF_PROTEIN_STABILITY, DODD_NASOPHARYNGEAL_CARCINOMA_UP, P300_01, chr20q11, GAVIN_FOXP3_TARGETS_CLUSTER_T7, WGTTNNNNNAAA_UNKNOWN

GO Biological Process (2): protein folding (GO:0006457), protein stabilization (GO:0050821)

GO Molecular Function (2): obsolete unfolded protein binding (GO:0051082), protein binding (GO:0005515)

GO Cellular Component (4): cytoplasm (GO:0005737), prefoldin complex (GO:0016272), protein folding chaperone complex (GO:0101031), RPAP3/R2TP/prefoldin-like complex (GO:1990062)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein-containing complex2
cellular process1
protein maturation1
regulation of protein stability1
binding1
intracellular anatomical structure1
cellular anatomical structure1
intracellular protein-containing complex1

Protein interactions and networks

STRING

712 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
PDRG1PFDN2Q9UHV9996
PDRG1PFDN6O15212995
PDRG1UXTQ9UBK9995
PDRG1DNAAF10Q96MX6984
PDRG1POLR2EP19388950
PDRG1RPAP3Q9H6T3857
PDRG1ASDURFL0R819793
PDRG1URI1O94763755
PDRG1PIH1D1Q9NWS0734
PDRG1RUVBL2Q9Y230671
PDRG1RUVBL1P82276663
PDRG1PFDN5Q99471601
PDRG1TP53P04637547
PDRG1SURF6O75683508
PDRG1SH3BP4Q9P0V3495

IntAct

127 interactions, top by confidence:

ABTypeScore
PARD6APRKCIpsi-mi:“MI:0914”(association)0.950
POLR2EPOLR3Apsi-mi:“MI:0914”(association)0.870
RUVBL1ZNHIT1psi-mi:“MI:0914”(association)0.860
PPP1CCCCDC85Cpsi-mi:“MI:0914”(association)0.740
PPP1CCCCDC85Cpsi-mi:“MI:2364”(proximity)0.740
PFDN2PDRG1psi-mi:“MI:0915”(physical association)0.740
PFDN4PFDN6psi-mi:“MI:0914”(association)0.730
POLR2EMED19psi-mi:“MI:0914”(association)0.730
RPRD1BPOLR2Dpsi-mi:“MI:0914”(association)0.730
POLR2GRECQL5psi-mi:“MI:0914”(association)0.730
PPP1CACCDC85Cpsi-mi:“MI:0914”(association)0.670
PPP1CACCDC85Cpsi-mi:“MI:2364”(proximity)0.670
PFDN2POLR3Apsi-mi:“MI:0914”(association)0.670
RUVBL1POLR3Apsi-mi:“MI:0914”(association)0.640
VBP1PFDN6psi-mi:“MI:0914”(association)0.640
PFDN1PFDN6psi-mi:“MI:0914”(association)0.640
DDB2CCT5psi-mi:“MI:0914”(association)0.640
POLR2LPOLR3Apsi-mi:“MI:0914”(association)0.640

BioGRID (181): PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS), ACY1 (Co-fractionation), URI1 (Co-fractionation), PDRG1 (Proximity Label-MS), PDRG1 (Proximity Label-MS), PDRG1 (Affinity Capture-MS), PDRG1 (Affinity Capture-MS)

ESM2 similar proteins: A0A1D5P556, A1A5P5, A7RX34, A7T0W1, A8WVJ9, A8XPL7, O18054, O94307, P40005, P46988, P48363, P57741, P59048, P61758, P61759, Q09305, Q0VIA1, Q10143, Q148L7, Q17827, Q21993, Q2KI89, Q2TBX2, Q3ZCF2, Q4R6W4, Q54JS0, Q54LS2, Q54ND3, Q5R629, Q5R6P5, Q5RCG9, Q5RFA9, Q61SU8, Q642A0, Q6CKH5, Q6DJ25, Q6GKV1, Q6IP67, Q8SYD0, Q9BTT4

Diamond homologs: P59048, Q148L7, Q5RFA9, Q642A0, Q9NUG6

SIGNOR signaling

1 interactions.

AEffectBMechanism
PDRG1“form complex”“URI1 prefoldin co-chaperone”binding

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 111 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
FGFR2 mutant receptor activation883.4×6e-13
RNA Polymerase III Chain Elongation978.2×7e-14
Signaling by FGFR2 IIIa TM865.9×5e-12
RNA Polymerase III Transcription Termination961.2×6e-13
RNA Polymerase III Transcription Initiation From Type 2 Promoter1057.9×7e-14
RNA Polymerase III Transcription Initiation From Type 1 Promoter1055.9×7e-14
RNA Polymerase III Transcription Initiation From Type 3 Promoter1055.9×7e-14
Telomere Maintenance1155.5×1e-14

GO biological processes:

GO termPartnersFoldFDR
protein dephosphorylation511.6×5e-03
protein folding1010.8×5e-06
protein stabilization1510.4×6e-09
transcription by RNA polymerase II96.6×8e-04

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance6
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

914 predictions. Top by Δscore:

VariantEffectΔscore
20:31945890:C:CCacceptor_gain1.0000
20:31946491:AATAC:Adonor_loss1.0000
20:31946492:ATACC:Adonor_loss1.0000
20:31946493:TACCT:Tdonor_loss1.0000
20:31946575:ATCTG:Aacceptor_loss1.0000
20:31946576:TCTGA:Tacceptor_loss1.0000
20:31946577:C:Aacceptor_loss1.0000
20:31946577:C:CCacceptor_gain1.0000
20:31946578:T:Aacceptor_loss1.0000
20:31946585:A:ACacceptor_gain1.0000
20:31948802:CCTTA:Cdonor_loss1.0000
20:31948803:CTTAC:Cdonor_loss1.0000
20:31948804:TTAC:Tdonor_loss1.0000
20:31948805:TACC:Tdonor_loss1.0000
20:31948806:A:ACdonor_gain1.0000
20:31948806:AC:Adonor_gain1.0000
20:31948806:ACCTT:Adonor_loss1.0000
20:31948807:C:CCdonor_gain1.0000
20:31948807:CC:Cdonor_gain1.0000
20:31948878:ATCTT:Aacceptor_gain1.0000
20:31948879:TCTT:Tacceptor_loss1.0000
20:31948880:CTT:Cacceptor_gain1.0000
20:31948880:CTTC:Cacceptor_loss1.0000
20:31948881:TT:Tacceptor_gain1.0000
20:31948881:TTCTG:Tacceptor_loss1.0000
20:31948882:TC:Tacceptor_loss1.0000
20:31948883:C:CCacceptor_gain1.0000
20:31948883:CTGA:Cacceptor_loss1.0000
20:31948884:T:Gacceptor_loss1.0000
20:31950305:AACTT:Adonor_loss1.0000

AlphaMissense

879 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
20:31950353:C:GR41P0.995
20:31946510:A:GL102P0.990
20:31950377:A:GL33P0.990
20:31946531:A:GL95P0.987
20:31946564:A:GL84P0.987
20:31945862:A:GL116S0.985
20:31946502:C:GA105P0.983
20:31946573:T:GQ81P0.981
20:31950364:C:AR37S0.981
20:31950364:C:GR37S0.981
20:31945872:C:GG113R0.980
20:31948851:A:CF65L0.980
20:31948851:A:TF65L0.980
20:31948852:A:GF65S0.980
20:31948853:A:GF65L0.980
20:31950344:A:GL44P0.980
20:31951904:C:GA20P0.980
20:31948870:A:TV59D0.978
20:31950348:C:GG43R0.978
20:31951903:G:TA20D0.978
20:31946540:C:GR92P0.975
20:31948861:C:AG62V0.973
20:31950339:C:GA46P0.973
20:31950354:G:CR41G0.973
20:31951924:A:GL13P0.973
20:31950335:A:GL47P0.972
20:31950347:C:TG43D0.972
20:31946543:A:GL91P0.968
20:31951891:A:GL24P0.967
20:31945853:A:TL119H0.966

dbSNP variants (sampled 300 via entrez): RS1000030839 (20:31952053 G>A), RS1000175146 (20:31947896 A>G), RS1000199095 (20:31943928 G>A), RS1000200999 (20:31953150 A>C), RS1000360235 (20:31949605 A>G), RS1000458580 (20:31947640 A>C), RS1000509425 (20:31949336 C>A), RS1000634054 (20:31948667 A>C), RS1000688065 (20:31948371 T>C), RS1000790529 (20:31949161 C>G), RS1001815065 (20:31951213 C>T), RS1002188327 (20:31950982 C>A,T), RS1002704865 (20:31944660 T>G), RS1002805296 (20:31951960 A>G), RS1002991506 (20:31945504 T>C)

Disease associations

OMIM: gene MIM:610789 | 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

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

ChemicalActions (top 5)PubMed papers
Cisplatindecreases expression, increases expression, affects cotreatment2
Cadmium Chlorideincreases abundance, increases expression2
aristolochic acid Iincreases expression1
ginger extractdecreases expression, increases abundance1
bisphenol Adecreases expression1
glycidyl methacrylateincreases expression1
sodium arseniteincreases expression1
butyraldehydeincreases expression1
potassium chromate(VI)affects cotreatment, increases expression1
epigallocatechin gallateaffects cotreatment, increases expression1
pentanalincreases expression1
di-n-butylphosphoric acidaffects expression1
perfluorooctane sulfonic aciddecreases expression1
abrineincreases expression1
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II)increases expression1
jinfukangaffects cotreatment, decreases expression1
PCI 5002affects cotreatment, increases expression1
Sunitinibdecreases expression1
Benzo(a)pyrenedecreases methylation1
Cadmiumincreases abundance, increases expression1
Copperaffects binding, decreases expression1
Dimethyl Sulfoxideincreases expression1
Disulfiramdecreases expression, affects binding1
Doxorubicinincreases expression1
Enzyme Inhibitorsincreases O-linked glycosylation, decreases activity1
Methyl Methanesulfonateincreases expression1
Oils, Volatiledecreases expression, increases abundance1
Rotenonedecreases expression1
Smokedecreases expression1
Thiramincreases 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.