PAGE5

gene
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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

FieldValue
HGNC IDHGNC:29992
Approved symbolPAGE5
NamePAGE family member 5
LocationXp11.21
Locus typegene with protein product
StatusApproved
AliasesPAGE-5, CT16.1, CT16.2
Ensembl geneENSG00000158639
Ensembl biotypeprotein_coding
OMIM301009
Entrez90737

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

ExonStartEnd
ENSE000014652425522398755224108
ENSE000014652505522034655220452
ENSE000017356185522262155222746
ENSE000017993305522176755221875
ENSE000034771645522137555221463

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 IDTPM avgSamples expressed
1964603.2079133
1964620.112037
1964610.094634

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047393.71gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099190.91gold quality
left testisUBERON:000453387.72gold quality
right testisUBERON:000453487.28gold quality
testisUBERON:000047386.13gold quality
spermCL:000001973.41gold quality
secondary oocyteCL:000065563.70gold quality
lateral nuclear group of thalamusUBERON:000273659.90gold quality
right lobe of liverUBERON:000111458.39gold quality
vena cavaUBERON:000408756.91gold quality
parotid glandUBERON:000183156.14gold quality
dorsal plus ventral thalamusUBERON:000189755.46gold quality
amniotic fluidUBERON:000017355.44gold quality
saphenous veinUBERON:000731855.44gold quality
pericardiumUBERON:000240755.22gold quality
nippleUBERON:000203055.16gold quality
subthalamic nucleusUBERON:000190654.93gold quality
layer of synovial tissueUBERON:000761654.92gold quality
urethraUBERON:000005754.90gold quality
trigeminal ganglionUBERON:000167554.85gold quality
pylorusUBERON:000116654.76gold quality
synovial jointUBERON:000221754.73gold quality
substantia nigra pars reticulataUBERON:000196654.68gold quality
thymusUBERON:000237054.67gold quality
substantia nigra pars compactaUBERON:000196554.65gold quality
dorsal root ganglionUBERON:000004454.60gold quality
ventral tegmental areaUBERON:000269154.52gold quality
tracheaUBERON:000312654.48gold quality
epithelium of nasopharynxUBERON:000195154.47gold quality
penisUBERON:000098954.41gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-GEOD-134144yes28.76
E-ANND-3no2.29

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-5582-3P99.8672.484221
HSA-MIR-579-3P99.8671.663628
HSA-MIR-548AR-3P99.8571.263889
HSA-MIR-664B-3P99.8471.653590
HSA-MIR-548AZ-3P99.8270.563549
HSA-MIR-548BC99.8270.613524
HSA-MIR-548E-3P99.8270.593514
HSA-MIR-548F-3P99.8270.593540
HSA-MIR-3180-5P99.8269.122422
HSA-MIR-548A-3P99.7670.583524
HSA-MIR-29B-2-5P99.6768.981726
HSA-MIR-6512-3P99.6566.071468
HSA-MIR-6720-5P99.6566.221459
HSA-MIR-548G-3P99.4868.672159
HSA-MIR-312399.4767.152693
HSA-MIR-16-2-3P99.2970.601954
HSA-MIR-195-3P99.2970.611954
HSA-MIR-4477A98.8369.752952
HSA-MIR-427498.5966.10630
HSA-MIR-338-3P98.1467.381137

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 5Q96GU1 (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 IDNamesCanonical?
Q96GU1-11yes
Q96GU1-22

RefSeq proteins (2): NP_001013453, NP_569734 (=MANE)

Domains & families (InterPro)

IDNameType
IPR008625GAGE_famFamily
IPR031320GAGEDomain

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)

ModelpLDDTFraction very-high
AF-Q96GU1-F161.280.00

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:

CategoryTerms
binding1

Protein interactions and networks

STRING

286 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
PAGE5PRSS50Q9UI38841
PAGE5SPA17Q15506720
PAGE5SAGE1Q9NXZ1720
PAGE5LIPIQ6XZB0665
PAGE5PER2O15055621
PAGE5MAGEC2Q9UBF1621
PAGE5ADAM2P78326610
PAGE5BMAL1O00327583
PAGE5CRY1Q16526541
PAGE5MAGEC1O60732506
PAGE5CLOCKO15516480
PAGE5XAGE5Q8WWM1476
PAGE5NR1D1P20393475
PAGE5CRY2Q49AN0475
PAGE5ACRBPQ8NEB7447

IntAct

13 interactions, top by confidence:

ABTypeScore
MEOX2PAGE5psi-mi:“MI:0915”(physical association)0.560
ERFTBL1Xpsi-mi:“MI:0914”(association)0.530
POT1PAGE5psi-mi:“MI:0915”(physical association)0.510
PAGE2PAGE5psi-mi:“MI:0915”(physical association)0.400
ZNF460ZNF320psi-mi:“MI:0914”(association)0.350
KRT83OFD1psi-mi:“MI:0914”(association)0.350
PRR15TNNC2psi-mi:“MI:0914”(association)0.350
FAM107BMAP9psi-mi:“MI:0914”(association)0.350
SPATA2LDCAF10psi-mi:“MI:0914”(association)0.350
POT1PAGE5psi-mi:“MI:0915”(physical association)0.000
PAGE5MEOX2psi-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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance17
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

555 predictions. Top by Δscore:

VariantEffectΔscore
X:55221373:A:AGacceptor_gain1.0000
X:55221374:G:GGacceptor_gain1.0000
X:55221460:GATT:Gdonor_gain1.0000
X:55221464:G:GGdonor_gain1.0000
X:55221882:G:GTdonor_gain1.0000
X:55221884:A:Tdonor_gain1.0000
X:55221909:G:GAdonor_gain1.0000
X:55222618:AAG:Aacceptor_gain1.0000
X:55222619:A:Gacceptor_gain1.0000
X:55222743:GCAG:Gdonor_gain1.0000
X:55222744:CAGG:Cdonor_loss1.0000
X:55222745:AGGT:Adonor_loss1.0000
X:55222746:GG:Gdonor_loss1.0000
X:55222747:G:GCdonor_loss1.0000
X:55222748:T:Adonor_loss1.0000
X:55220449:GCCG:Gdonor_gain0.9900
X:55221369:TTTCA:Tacceptor_loss0.9900
X:55221370:TTCAG:Tacceptor_loss0.9900
X:55221371:TCAGT:Tacceptor_loss0.9900
X:55221372:CAGTG:Cacceptor_gain0.9900
X:55221373:A:ACacceptor_loss0.9900
X:55221373:AGT:Aacceptor_gain0.9900
X:55221373:AGTGA:Aacceptor_gain0.9900
X:55221374:G:Aacceptor_loss0.9900
X:55221374:GT:Gacceptor_gain0.9900
X:55221374:GTG:Gacceptor_gain0.9900
X:55221374:GTGA:Gacceptor_gain0.9900
X:55221374:GTGAG:Gacceptor_gain0.9900
X:55221462:TT:Tdonor_gain0.9900
X:55221748:C:Gacceptor_gain0.9900

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):

StudyTraitp-value
GCST006661_51Male-pattern baldness5.000000e-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.

ChemicalActions (top 5)PubMed papers
zinc chromateincreases abundance, increases expression1
chromium hexavalent ionincreases abundance, increases expression1
CGP 52608affects binding, increases reaction1
clothianidindecreases expression1
Resveratrolaffects cotreatment, decreases expression1
Decitabineincreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Plant Extractsaffects cotreatment, decreases expression1
Silicon Dioxideincreases 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.