PAGE5
gene geneOn this page
Also known as PAGE-5CT16.1CT16.2
Summary
PAGE5 (PAGE family member 5, HGNC:29992) is a protein-coding gene on chromosome Xp11.21, encoding P antigen family member 5 (Q96GU1).
This gene is a member of family of proteins that are expressed in a variety of tumors and in some fetal and reproductive tissues. The encoded protein may protect cells from programmed cell death. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found.
Source: NCBI Gene 90737 — RefSeq curated summary.
At a glance
- GWAS associations: 1
- Clinical variants (ClinVar): 22 total
- MANE Select transcript:
NM_001013435
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:29992 |
| Approved symbol | PAGE5 |
| Name | PAGE family member 5 |
| Location | Xp11.21 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | PAGE-5, CT16.1, CT16.2 |
| Ensembl gene | ENSG00000158639 |
| Ensembl biotype | protein_coding |
| OMIM | 301009 |
| Entrez | 90737 |
Gene structure
Transcript identifiers
Ensembl transcripts: 3 — 3 protein_coding
ENST00000289619, ENST00000374952, ENST00000374955
RefSeq mRNA: 2 — MANE Select: NM_001013435
NM_001013435, NM_130467
CCDS: CCDS14368, CCDS35306
Canonical transcript exons
ENST00000374955 — 5 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001465242 | 55223987 | 55224108 |
| ENSE00001465250 | 55220346 | 55220452 |
| ENSE00001735618 | 55222621 | 55222746 |
| ENSE00001799330 | 55221767 | 55221875 |
| ENSE00003477164 | 55221375 | 55221463 |
Expression profiles
Bgee: expression breadth broad, 91 present calls, max score 93.71.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 3.4146 / max 350.6766, expressed in 140 samples.
FANTOM5 promoters (3 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 196460 | 3.2079 | 133 |
| 196462 | 0.1120 | 37 |
| 196461 | 0.0946 | 34 |
Top tissues by expression
217 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 93.71 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 90.91 | gold quality |
| left testis | UBERON:0004533 | 87.72 | gold quality |
| right testis | UBERON:0004534 | 87.28 | gold quality |
| testis | UBERON:0000473 | 86.13 | gold quality |
| sperm | CL:0000019 | 73.41 | gold quality |
| secondary oocyte | CL:0000655 | 63.70 | gold quality |
| lateral nuclear group of thalamus | UBERON:0002736 | 59.90 | gold quality |
| right lobe of liver | UBERON:0001114 | 58.39 | gold quality |
| vena cava | UBERON:0004087 | 56.91 | gold quality |
| parotid gland | UBERON:0001831 | 56.14 | gold quality |
| dorsal plus ventral thalamus | UBERON:0001897 | 55.46 | gold quality |
| amniotic fluid | UBERON:0000173 | 55.44 | gold quality |
| saphenous vein | UBERON:0007318 | 55.44 | gold quality |
| pericardium | UBERON:0002407 | 55.22 | gold quality |
| nipple | UBERON:0002030 | 55.16 | gold quality |
| subthalamic nucleus | UBERON:0001906 | 54.93 | gold quality |
| layer of synovial tissue | UBERON:0007616 | 54.92 | gold quality |
| urethra | UBERON:0000057 | 54.90 | gold quality |
| trigeminal ganglion | UBERON:0001675 | 54.85 | gold quality |
| pylorus | UBERON:0001166 | 54.76 | gold quality |
| synovial joint | UBERON:0002217 | 54.73 | gold quality |
| substantia nigra pars reticulata | UBERON:0001966 | 54.68 | gold quality |
| thymus | UBERON:0002370 | 54.67 | gold quality |
| substantia nigra pars compacta | UBERON:0001965 | 54.65 | gold quality |
| dorsal root ganglion | UBERON:0000044 | 54.60 | gold quality |
| ventral tegmental area | UBERON:0002691 | 54.52 | gold quality |
| trachea | UBERON:0003126 | 54.48 | gold quality |
| epithelium of nasopharynx | UBERON:0001951 | 54.47 | gold quality |
| penis | UBERON:0000989 | 54.41 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-134144 | yes | 28.76 |
| E-ANND-3 | no | 2.29 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
20 targeting PAGE5, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-5582-3P | 99.86 | 72.48 | 4221 |
| HSA-MIR-579-3P | 99.86 | 71.66 | 3628 |
| HSA-MIR-548AR-3P | 99.85 | 71.26 | 3889 |
| HSA-MIR-664B-3P | 99.84 | 71.65 | 3590 |
| HSA-MIR-548AZ-3P | 99.82 | 70.56 | 3549 |
| HSA-MIR-548BC | 99.82 | 70.61 | 3524 |
| HSA-MIR-548E-3P | 99.82 | 70.59 | 3514 |
| HSA-MIR-548F-3P | 99.82 | 70.59 | 3540 |
| HSA-MIR-3180-5P | 99.82 | 69.12 | 2422 |
| HSA-MIR-548A-3P | 99.76 | 70.58 | 3524 |
| HSA-MIR-29B-2-5P | 99.67 | 68.98 | 1726 |
| HSA-MIR-6512-3P | 99.65 | 66.07 | 1468 |
| HSA-MIR-6720-5P | 99.65 | 66.22 | 1459 |
| HSA-MIR-548G-3P | 99.48 | 68.67 | 2159 |
| HSA-MIR-3123 | 99.47 | 67.15 | 2693 |
| HSA-MIR-16-2-3P | 99.29 | 70.60 | 1954 |
| HSA-MIR-195-3P | 99.29 | 70.61 | 1954 |
| HSA-MIR-4477A | 98.83 | 69.75 | 2952 |
| HSA-MIR-4274 | 98.59 | 66.10 | 630 |
| HSA-MIR-338-3P | 98.14 | 67.38 | 1137 |
Literature-anchored findings (GeneRIF, showing 1)
- Results indicate that CT16 promotes the survival of melanoma cells and is therefore a potential target for future drug development. (PMID:23028975)
Cross-species orthologs
0 orthologs
Paralogs (22): PAGE1 (ENSG00000068985), PAGE4 (ENSG00000101951), XAGE2 (ENSG00000155622), XAGE3 (ENSG00000171402), XAGE5 (ENSG00000171405), GAGE2A (ENSG00000189064), PAGE3 (ENSG00000204279), XAGE1A (ENSG00000204379), XAGE1B (ENSG00000204382), GAGE1 (ENSG00000205777), GAGE12G (ENSG00000215269), GAGE10 (ENSG00000215274), GAGE12E (ENSG00000216649), GAGE12J (ENSG00000224659), GAGE12H (ENSG00000224902), GAGE12D (ENSG00000227488), PAGE2 (ENSG00000234068), GAGE12F (ENSG00000236362), GAGE12C (ENSG00000237671), PAGE2B (ENSG00000238269), GAGE13 (ENSG00000274274), GAGE2E (ENSG00000275113)
Protein
Protein identifiers
P antigen family member 5 — Q96GU1 (reviewed: Q96GU1)
Alternative names: Cancer/testis antigen 16.1, G antigen family E member 1, Prostate-associated gene 5 protein
All UniProt accessions (2): Q96GU1, Q5JUL1
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the GAGE family.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q96GU1-1 | 1 | yes |
| Q96GU1-2 | 2 |
RefSeq proteins (2): NP_001013453, NP_569734 (=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR008625 | GAGE_fam | Family |
| IPR031320 | GAGE | Domain |
Pfam: PF05831
UniProt features (8 total): region of interest 2, compositionally biased region 2, modified residue 2, chain 1, splice variant 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q96GU1-F1 | 61.28 | 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 (2): 113, 116
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 15 (showing top):
ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, chrXp11, RATTENBACHER_BOUND_BY_CELF1, ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, ZNF507_TARGET_GENES, ZNF766_TARGET_GENES, MIR5582_3P, MIR4477A, MIR338_3P, MIR4274, GSE18791_CTRL_VS_NEWCASTLE_VIRUS_DC_1H_DN, PULVER_FOREY_PERTURB_ACCUMULATION_G1_S, GSE2770_IL12_ACT_VS_ACT_CD4_TCELL_6H_UP, GSE21670_IL6_VS_TGFB_AND_IL6_TREATED_CD4_TCELL_UP, GSE21927_SPLEEN_VS_TUMOR_MONOCYTE_C57BL6_DN
GO Biological Process (0):
GO Molecular Function (1): protein binding (GO:0005515)
GO Cellular Component (0):
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| binding | 1 |
Protein interactions and networks
STRING
286 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| PAGE5 | PRSS50 | Q9UI38 | 841 |
| PAGE5 | SPA17 | Q15506 | 720 |
| PAGE5 | SAGE1 | Q9NXZ1 | 720 |
| PAGE5 | LIPI | Q6XZB0 | 665 |
| PAGE5 | PER2 | O15055 | 621 |
| PAGE5 | MAGEC2 | Q9UBF1 | 621 |
| PAGE5 | ADAM2 | P78326 | 610 |
| PAGE5 | BMAL1 | O00327 | 583 |
| PAGE5 | CRY1 | Q16526 | 541 |
| PAGE5 | MAGEC1 | O60732 | 506 |
| PAGE5 | CLOCK | O15516 | 480 |
| PAGE5 | XAGE5 | Q8WWM1 | 476 |
| PAGE5 | NR1D1 | P20393 | 475 |
| PAGE5 | CRY2 | Q49AN0 | 475 |
| PAGE5 | ACRBP | Q8NEB7 | 447 |
IntAct
13 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| MEOX2 | PAGE5 | psi-mi:“MI:0915”(physical association) | 0.560 |
| ERF | TBL1X | psi-mi:“MI:0914”(association) | 0.530 |
| POT1 | PAGE5 | psi-mi:“MI:0915”(physical association) | 0.510 |
| PAGE2 | PAGE5 | psi-mi:“MI:0915”(physical association) | 0.400 |
| ZNF460 | ZNF320 | psi-mi:“MI:0914”(association) | 0.350 |
| KRT83 | OFD1 | psi-mi:“MI:0914”(association) | 0.350 |
| PRR15 | TNNC2 | psi-mi:“MI:0914”(association) | 0.350 |
| FAM107B | MAP9 | psi-mi:“MI:0914”(association) | 0.350 |
| SPATA2L | DCAF10 | psi-mi:“MI:0914”(association) | 0.350 |
| POT1 | PAGE5 | psi-mi:“MI:0915”(physical association) | 0.000 |
| PAGE5 | MEOX2 | psi-mi:“MI:0915”(physical association) | 0.000 |
BioGRID (12): PAGE5 (Proximity Label-MS), PAGE5 (Two-hybrid), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Affinity Capture-MS), PAGE5 (Two-hybrid)
ESM2 similar proteins: A1L429, A6NDE8, A6NER3, A6NGK3, O41801, O55777, O60829, O75459, O76087, P03204, P04611, P06937, P0CL80, P0CL81, P0CL82, P0DSO3, P0DTW1, P18804, P22421, P86478, P86479, P86480, P86481, P86496, Q13066, Q13069, Q13070, Q2T9P9, Q3KST0, Q4V321, Q4V326, Q5JRK9, Q5JUK9, Q6AY45, Q6I7R5, Q6IPX3, Q6NT46, Q7Z2X7, Q8AIH8, Q8CCT4
Diamond homologs: O75459, Q5JRK9, Q5JUK9, Q7Z2X7, Q8WTP9, Q8WWM1, Q96GT9, Q96GU1, A6NGK3
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
22 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 17 |
| Likely benign | 1 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
555 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| X:55221373:A:AG | acceptor_gain | 1.0000 |
| X:55221374:G:GG | acceptor_gain | 1.0000 |
| X:55221460:GATT:G | donor_gain | 1.0000 |
| X:55221464:G:GG | donor_gain | 1.0000 |
| X:55221882:G:GT | donor_gain | 1.0000 |
| X:55221884:A:T | donor_gain | 1.0000 |
| X:55221909:G:GA | donor_gain | 1.0000 |
| X:55222618:AAG:A | acceptor_gain | 1.0000 |
| X:55222619:A:G | acceptor_gain | 1.0000 |
| X:55222743:GCAG:G | donor_gain | 1.0000 |
| X:55222744:CAGG:C | donor_loss | 1.0000 |
| X:55222745:AGGT:A | donor_loss | 1.0000 |
| X:55222746:GG:G | donor_loss | 1.0000 |
| X:55222747:G:GC | donor_loss | 1.0000 |
| X:55222748:T:A | donor_loss | 1.0000 |
| X:55220449:GCCG:G | donor_gain | 0.9900 |
| X:55221369:TTTCA:T | acceptor_loss | 0.9900 |
| X:55221370:TTCAG:T | acceptor_loss | 0.9900 |
| X:55221371:TCAGT:T | acceptor_loss | 0.9900 |
| X:55221372:CAGTG:C | acceptor_gain | 0.9900 |
| X:55221373:A:AC | acceptor_loss | 0.9900 |
| X:55221373:AGT:A | acceptor_gain | 0.9900 |
| X:55221373:AGTGA:A | acceptor_gain | 0.9900 |
| X:55221374:G:A | acceptor_loss | 0.9900 |
| X:55221374:GT:G | acceptor_gain | 0.9900 |
| X:55221374:GTG:G | acceptor_gain | 0.9900 |
| X:55221374:GTGA:G | acceptor_gain | 0.9900 |
| X:55221374:GTGAG:G | acceptor_gain | 0.9900 |
| X:55221462:TT:T | donor_gain | 0.9900 |
| X:55221748:C:G | acceptor_gain | 0.9900 |
AlphaMissense
709 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000290960 (X:55222856 A>G), RS1001364645 (X:55223123 A>G), RS1006110822 (X:55224286 A>G), RS1006367825 (X:55221172 T>A), RS1007322454 (X:55222276 TTAA>T), RS1008941643 (X:55224152 T>C), RS1010964281 (X:55220816 G>T), RS1011845276 (X:55218768 T>C), RS1014079644 (X:55222439 G>A), RS1014825922 (X:55224318 T>C), RS1016042543 (X:55220705 G>A,C,T), RS1016121669 (X:55218397 G>A), RS1016838651 (X:55221177 T>C), RS1017556955 (X:55221391 G>T), RS1018948643 (X:55224165 A>C,G)
Disease associations
OMIM: gene MIM:301009 | 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):
| Study | Trait | p-value |
|---|---|---|
| GCST006661_51 | Male-pattern baldness | 5.000000e-10 |
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
9 total (human), top 9 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| zinc chromate | increases abundance, increases expression | 1 |
| chromium hexavalent ion | increases abundance, increases expression | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| clothianidin | decreases expression | 1 |
| Resveratrol | affects cotreatment, decreases expression | 1 |
| Decitabine | increases expression | 1 |
| Benzo(a)pyrene | affects methylation, decreases methylation | 1 |
| Plant Extracts | affects cotreatment, decreases expression | 1 |
| Silicon Dioxide | 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.