DERPC
gene geneOn this page
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
| Field | Value |
|---|---|
| HGNC ID | HGNC:54084 |
| Approved symbol | DERPC |
| Name | DERPC proline and glycine rich nuclear protein |
| Location | 16q22.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000286140 |
| Ensembl biotype | protein_coding |
| OMIM | 621352 |
| Entrez | 113455421 |
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
| Exon | Start | End |
|---|---|---|
| ENSE00003606231 | 69118010 | 69120649 |
| ENSE00003846850 | 69121436 | 69121493 |
| ENSE00003923433 | 69132484 | 69132588 |
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 ID | TPM avg | Samples expressed |
|---|---|---|
| 157891 | 51.5794 | 1820 |
| 157890 | 1.9919 | 1160 |
Top tissues by expression
133 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| ganglionic eminence | UBERON:0004023 | 88.38 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 87.63 | gold quality |
| ventricular zone | UBERON:0003053 | 87.32 | gold quality |
| placenta | UBERON:0001987 | 86.70 | gold quality |
| granulocyte | CL:0000094 | 86.58 | gold quality |
| lymph node | UBERON:0000029 | 85.71 | gold quality |
| cortical plate | UBERON:0005343 | 84.86 | gold quality |
| right lobe of liver | UBERON:0001114 | 84.66 | gold quality |
| vermiform appendix | UBERON:0001154 | 84.14 | gold quality |
| colonic epithelium | UBERON:0000397 | 83.90 | gold quality |
| apex of heart | UBERON:0002098 | 83.82 | gold quality |
| lower esophagus mucosa | UBERON:0035834 | 83.20 | gold quality |
| right uterine tube | UBERON:0001302 | 83.10 | gold quality |
| spleen | UBERON:0002106 | 82.90 | gold quality |
| islet of Langerhans | UBERON:0000006 | 82.85 | gold quality |
| gall bladder | UBERON:0002110 | 82.46 | gold quality |
| fallopian tube | UBERON:0003889 | 82.37 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 82.27 | gold quality |
| metanephros cortex | UBERON:0010533 | 82.11 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 81.79 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 81.78 | gold quality |
| urinary bladder | UBERON:0001255 | 81.64 | gold quality |
| skin of leg | UBERON:0001511 | 81.60 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 81.54 | gold quality |
| heart left ventricle | UBERON:0002084 | 81.30 | gold quality |
| esophagus mucosa | UBERON:0002469 | 81.28 | gold quality |
| zone of skin | UBERON:0000014 | 81.16 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 81.12 | gold quality |
| esophagus | UBERON:0001043 | 80.95 | gold quality |
| right coronary artery | UBERON:0001625 | 80.89 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.46 |
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
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Derpc | ENSMUSG00000117748 |
| rattus_norvegicus | Chtf8 | ENSRNOG00000047246 |
Protein
Protein identifiers
Decreased expression in renal and prostate cancer protein — P0CG12 (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)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0CG12-F1 | 46.73 | 0.00 |
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:
| Category | Terms |
|---|---|
| nuclear lumen | 1 |
| cellular anatomical structure | 1 |
| extracellular vesicle | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
176 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| DERPC | DPEP1 | P16444 | 507 |
| DERPC | RFC1 | P35251 | 296 |
| DERPC | CHTF18 | Q8WVB6 | 280 |
| DERPC | CTCF | P49711 | 270 |
| DERPC | CDH17 | Q12864 | 221 |
| DERPC | RNF138 | Q8WVD3 | 166 |
| DERPC | UHRF2 | Q96PU4 | 166 |
| DERPC | RNF113A | O15541 | 166 |
| DERPC | TCEA1 | P23193 | 166 |
| DERPC | CCDC82 | Q8N4S0 | 161 |
| DERPC | CDH1 | P12830 | 149 |
| DERPC | PPM1G | O15355 | 140 |
| DERPC | RFC3 | P40938 | 132 |
| DERPC | UHRF1 | Q96T88 | 116 |
| DERPC | NCOA5 | Q9HCD5 | 90 |
IntAct
6 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| Cdc20 | BUB1 | psi-mi:“MI:0914”(association) | 0.560 |
| Prkcz | GOLIM4 | psi-mi:“MI:0914”(association) | 0.350 |
| UBA1 | NVL | psi-mi:“MI:0914”(association) | 0.350 |
| ESR1 | ESYT2 | psi-mi:“MI:0914”(association) | 0.350 |
| KLHL22 | TRAV18 | psi-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):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 1 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
568 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 16:69121166:TCGCA:T | acceptor_gain | 1.0000 |
| 16:69121167:CGCA:C | acceptor_gain | 1.0000 |
| 16:69121167:CGCAC:C | acceptor_gain | 1.0000 |
| 16:69121168:GCA:G | acceptor_gain | 1.0000 |
| 16:69121169:CA:C | acceptor_gain | 1.0000 |
| 16:69121169:CAC:C | acceptor_gain | 1.0000 |
| 16:69121170:ACTG:A | acceptor_loss | 1.0000 |
| 16:69121171:C:CA | acceptor_loss | 1.0000 |
| 16:69121171:C:CC | acceptor_gain | 1.0000 |
| 16:69121431:CTTA:C | donor_loss | 1.0000 |
| 16:69121432:TTA:T | donor_loss | 1.0000 |
| 16:69121433:TA:T | donor_loss | 1.0000 |
| 16:69121434:ACC:A | donor_loss | 1.0000 |
| 16:69121435:C:CG | donor_loss | 1.0000 |
| 16:69121489:ACAAG:A | acceptor_gain | 1.0000 |
| 16:69121490:CAAG:C | acceptor_gain | 1.0000 |
| 16:69121490:CAAGC:C | acceptor_gain | 1.0000 |
| 16:69121491:AAG:A | acceptor_gain | 1.0000 |
| 16:69121492:AG:A | acceptor_gain | 1.0000 |
| 16:69121492:AGC:A | acceptor_loss | 1.0000 |
| 16:69121493:GC:G | acceptor_loss | 1.0000 |
| 16:69121494:C:CC | acceptor_gain | 1.0000 |
| 16:69121494:C:T | acceptor_loss | 1.0000 |
| 16:69121495:T:A | acceptor_loss | 1.0000 |
| 16:69120649:CCTT:C | acceptor_gain | 0.9900 |
| 16:69121048:CTCA:C | donor_loss | 0.9900 |
| 16:69121051:A:T | donor_loss | 0.9900 |
| 16:69121052:C:CT | donor_loss | 0.9900 |
| 16:69121430:ACTT:A | donor_loss | 0.9900 |
| 16:69121434:A:AC | donor_gain | 0.9900 |
AlphaMissense
3288 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 16:69120384:C:A | W15C | 0.953 |
| 16:69120384:C:G | W15C | 0.953 |
| 16:69120386:A:G | W15R | 0.952 |
| 16:69120386:A:T | W15R | 0.952 |
| 16:69118953:A:C | F492L | 0.947 |
| 16:69118953:A:T | F492L | 0.947 |
| 16:69118955:A:G | F492L | 0.947 |
| 16:69119274:G:C | F385L | 0.922 |
| 16:69119274:G:T | F385L | 0.922 |
| 16:69119276:A:G | F385L | 0.922 |
| 16:69118911:G:C | F506L | 0.917 |
| 16:69118911:G:T | F506L | 0.917 |
| 16:69118913:A:G | F506L | 0.917 |
| 16:69119190:G:C | F413L | 0.916 |
| 16:69119190:G:T | F413L | 0.916 |
| 16:69119192:A:G | F413L | 0.916 |
| 16:69119596:A:G | I278T | 0.916 |
| 16:69120408:G:C | F7L | 0.916 |
| 16:69120408:G:T | F7L | 0.916 |
| 16:69120410:A:G | F7L | 0.916 |
| 16:69120276:G:C | F51L | 0.912 |
| 16:69120276:G:T | F51L | 0.912 |
| 16:69120278:A:G | F51L | 0.912 |
| 16:69119343:A:C | F362L | 0.911 |
| 16:69119343:A:T | F362L | 0.911 |
| 16:69119345:A:G | F362L | 0.911 |
| 16:69119232:G:C | F399L | 0.909 |
| 16:69119232:G:T | F399L | 0.909 |
| 16:69119234:A:G | F399L | 0.909 |
| 16:69120424:T:A | K2I | 0.908 |
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.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| Cadmium Chloride | increases expression | 1 |
| Okadaic Acid | increases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.