DERPC

gene
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Summary

DERPC (DERPC proline and glycine rich nuclear protein, HGNC:54084) is a protein-coding gene on chromosome 16q22.1, encoding Decreased expression in renal and prostate cancer protein (P0CG12). Potential tumor suppressor.

Located in nucleoplasm.

Source: NCBI Gene 113455421 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_001002847

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:54084
Approved symbolDERPC
NameDERPC proline and glycine rich nuclear protein
Location16q22.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000286140
Ensembl biotypeprotein_coding
OMIM621352
Entrez113455421

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000306585, ENST00000519520

RefSeq mRNA: 7 — MANE Select: NM_001002847 NM_001002847, NM_001040144, NM_001366602, NM_001366603, NM_001366604, NM_001366605, NM_001366606

CCDS: CCDS92188

Canonical transcript exons

ENST00000519520 — 3 exons

ExonStartEnd
ENSE000036062316911801069120649
ENSE000038468506912143669121493
ENSE000039234336913248469132588

Expression profiles

Bgee: expression breadth ubiquitous, 133 present calls, max score 88.38.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 51.5794 / max 263.1907, expressed in 1820 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
15789151.57941820
1578901.99191160

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
ganglionic eminenceUBERON:000402388.38gold quality
mucosa of transverse colonUBERON:000499187.63gold quality
ventricular zoneUBERON:000305387.32gold quality
placentaUBERON:000198786.70gold quality
granulocyteCL:000009486.58gold quality
lymph nodeUBERON:000002985.71gold quality
cortical plateUBERON:000534384.86gold quality
right lobe of liverUBERON:000111484.66gold quality
vermiform appendixUBERON:000115484.14gold quality
colonic epitheliumUBERON:000039783.90gold quality
apex of heartUBERON:000209883.82gold quality
lower esophagus mucosaUBERON:003583483.20gold quality
right uterine tubeUBERON:000130283.10gold quality
spleenUBERON:000210682.90gold quality
islet of LangerhansUBERON:000000682.85gold quality
gall bladderUBERON:000211082.46gold quality
fallopian tubeUBERON:000388982.37gold quality
adult mammalian kidneyUBERON:000008282.27gold quality
metanephros cortexUBERON:001053382.11gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047381.79gold quality
smooth muscle tissueUBERON:000113581.78gold quality
urinary bladderUBERON:000125581.64gold quality
skin of legUBERON:000151181.60gold quality
right lobe of thyroid glandUBERON:000111981.54gold quality
heart left ventricleUBERON:000208481.30gold quality
esophagus mucosaUBERON:000246981.28gold quality
zone of skinUBERON:000001481.16gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099181.12gold quality
esophagusUBERON:000104380.95gold quality
right coronary arteryUBERON:000162580.89gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.46

Regulation

Is transcription factor: no

Literature-anchored findings (GeneRIF, showing 1)

  • decreased expression of DERPC may be implicated in tumorigenesis of prostate and renal tumors (PMID:12477976)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusDerpcENSMUSG00000117748
rattus_norvegicusChtf8ENSRNOG00000047246

Protein

Protein identifiers

Decreased expression in renal and prostate cancer proteinP0CG12 (reviewed: P0CG12)

All UniProt accessions (2): P0CG12, L0R4W3

UniProt curated annotations — full annotation on UniProt →

Function. Potential tumor suppressor. Inhibits prostate tumor cell growth, when overexpressed.

Subcellular location. Nucleus.

Tissue specificity. Ubiquitously expressed, with abundant expression in kidney, skeletal muscle, testis, liver, ovary, and heart and moderate expression in prostate. Expression is significantly reduced in renal and prostate tumors. No differential expression in breast cancer cells, between lobular carcinoma and normal lobules.

Miscellaneous. Found in a common chromosomal region of deletion in breast cancer.

Similarity. Belongs to the DERPC family.

RefSeq proteins (7): NP_001002847, NP_001035234, NP_001353531, NP_001353532, NP_001353533, NP_001353534, NP_001353535 (=MANE)

Domains & families (InterPro)

UniProt features (12 total): modified residue 4, compositionally biased region 4, region of interest 3, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0CG12-F146.730.00

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 (4): 387, 423, 302, 364

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 11 (showing top): chr16q22, CAGGTCC_MIR492, CAGCTTT_MIR320, FEVR_CTNNB1_TARGETS_DN, CTCAGGG_MIR125B_MIR125A, MOHANKUMAR_HOXA1_TARGETS_UP, ZHANG_FH_DEFICIENT_RCC_C2_VS_OTHERS_UP, GENES_CORRELATED_WITH_MN1_DELETION, GENES_CORRELATED_WITH_PDGFRB_DELETION, GCTTGAA_MIR498, CACTGTG_MIR128A_MIR128B

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (3): nucleoplasm (GO:0005654), extracellular exosome (GO:0070062), nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
nuclear lumen1
cellular anatomical structure1
extracellular vesicle1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

176 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
DERPCDPEP1P16444507
DERPCRFC1P35251296
DERPCCHTF18Q8WVB6280
DERPCCTCFP49711270
DERPCCDH17Q12864221
DERPCRNF138Q8WVD3166
DERPCUHRF2Q96PU4166
DERPCRNF113AO15541166
DERPCTCEA1P23193166
DERPCCCDC82Q8N4S0161
DERPCCDH1P12830149
DERPCPPM1GO15355140
DERPCRFC3P40938132
DERPCUHRF1Q96T88116
DERPCNCOA5Q9HCD590

IntAct

6 interactions, top by confidence:

ABTypeScore
Cdc20BUB1psi-mi:“MI:0914”(association)0.560
PrkczGOLIM4psi-mi:“MI:0914”(association)0.350
UBA1NVLpsi-mi:“MI:0914”(association)0.350
ESR1ESYT2psi-mi:“MI:0914”(association)0.350
KLHL22TRAV18psi-mi:“MI:0914”(association)0.350

ESM2 similar proteins: A5PJN8, B1AYB6, B2RWS6, B2RYL1, C7EMF5, F4I171, O48582, O55196, O75157, P0CG10, P0CG12, P0CG14, P18583, P45481, P49750, P62500, P62501, Q09472, Q10571, Q14686, Q148B6, Q15428, Q29W20, Q32KG4, Q3HS82, Q4R837, Q5E9L3, Q5ISE2, Q5JT82, Q5PRE5, Q5R623, Q62203, Q66IN2, Q6JHU9, Q6UX39, Q76KD6, Q86XN7, Q8BH93, Q8NDC0, Q91012

Diamond homologs: B2RYL1, P0CG10, P0CG12, P0CG14

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 significance0
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

568 predictions. Top by Δscore:

VariantEffectΔscore
16:69121166:TCGCA:Tacceptor_gain1.0000
16:69121167:CGCA:Cacceptor_gain1.0000
16:69121167:CGCAC:Cacceptor_gain1.0000
16:69121168:GCA:Gacceptor_gain1.0000
16:69121169:CA:Cacceptor_gain1.0000
16:69121169:CAC:Cacceptor_gain1.0000
16:69121170:ACTG:Aacceptor_loss1.0000
16:69121171:C:CAacceptor_loss1.0000
16:69121171:C:CCacceptor_gain1.0000
16:69121431:CTTA:Cdonor_loss1.0000
16:69121432:TTA:Tdonor_loss1.0000
16:69121433:TA:Tdonor_loss1.0000
16:69121434:ACC:Adonor_loss1.0000
16:69121435:C:CGdonor_loss1.0000
16:69121489:ACAAG:Aacceptor_gain1.0000
16:69121490:CAAG:Cacceptor_gain1.0000
16:69121490:CAAGC:Cacceptor_gain1.0000
16:69121491:AAG:Aacceptor_gain1.0000
16:69121492:AG:Aacceptor_gain1.0000
16:69121492:AGC:Aacceptor_loss1.0000
16:69121493:GC:Gacceptor_loss1.0000
16:69121494:C:CCacceptor_gain1.0000
16:69121494:C:Tacceptor_loss1.0000
16:69121495:T:Aacceptor_loss1.0000
16:69120649:CCTT:Cacceptor_gain0.9900
16:69121048:CTCA:Cdonor_loss0.9900
16:69121051:A:Tdonor_loss0.9900
16:69121052:C:CTdonor_loss0.9900
16:69121430:ACTT:Adonor_loss0.9900
16:69121434:A:ACdonor_gain0.9900

AlphaMissense

3288 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:69120384:C:AW15C0.953
16:69120384:C:GW15C0.953
16:69120386:A:GW15R0.952
16:69120386:A:TW15R0.952
16:69118953:A:CF492L0.947
16:69118953:A:TF492L0.947
16:69118955:A:GF492L0.947
16:69119274:G:CF385L0.922
16:69119274:G:TF385L0.922
16:69119276:A:GF385L0.922
16:69118911:G:CF506L0.917
16:69118911:G:TF506L0.917
16:69118913:A:GF506L0.917
16:69119190:G:CF413L0.916
16:69119190:G:TF413L0.916
16:69119192:A:GF413L0.916
16:69119596:A:GI278T0.916
16:69120408:G:CF7L0.916
16:69120408:G:TF7L0.916
16:69120410:A:GF7L0.916
16:69120276:G:CF51L0.912
16:69120276:G:TF51L0.912
16:69120278:A:GF51L0.912
16:69119343:A:CF362L0.911
16:69119343:A:TF362L0.911
16:69119345:A:GF362L0.911
16:69119232:G:CF399L0.909
16:69119232:G:TF399L0.909
16:69119234:A:GF399L0.909
16:69120424:T:AK2I0.908

dbSNP variants (sampled 300 via entrez): RS1000311617 (16:69119977 G>A,C), RS1000537458 (16:69130925 T>C), RS1000769290 (16:69130528 C>A), RS1000915406 (16:69134408 G>C), RS1001210112 (16:69122032 C>A,T), RS1001282816 (16:69125686 A>C,G), RS1001868649 (16:69125805 G>A,C), RS1001898988 (16:69131595 C>A,G), RS1002171595 (16:69129710 TCTC>T), RS1002359386 (16:69126055 A>G), RS1002374308 (16:69131869 A>T), RS1002433966 (16:69117915 G>A), RS1002568418 (16:69134182 G>A), RS1002621283 (16:69120871 T>C), RS1002887875 (16:69118625 T>C)

Disease associations

OMIM: gene MIM:621352 | 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

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
Cadmium Chlorideincreases expression1
Okadaic Acidincreases 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.