PAGR1
PAXIP1-associated glutamate-rich protein 1
Also known as: C16orf53, GAS, MGC4606, PA1, PAGR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BTK6
- Gene
- PAGR1
- Ensembl
- ENSG00000280789
- Chromosome
- 16
- Canonical length
- 254 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables nuclear estrogen receptor binding activity. Involved in positive regulation of cell cycle G1/S phase transition; positive regulation of intracellular estrogen receptor signaling pathway; and positive regulation of transcription by RNA polymerase II. Located in nucleus. Part of MLL3/4 complex. Biomarker of esophagus squamous cell carcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
254 residues, UniProt reviewed canonical sequence.
>Q9BTK6|PAGR1
1 MSLARGHGDT AASTAAPLSE EGEVTSGLQA LAVEDTGGPS ASAGKAEDEG EGGREETERE
61 GSGGEEAQGE VPSAGGEEPA EEDSEDWCVP CSDEEVELPA DGQPWMPPPS EIQRLYELLA
121 AHGTLELQAE ILPRRPPTPE AQSEEERSDE EPEAKEEEEE KPHMPTEFDF DDEPVTPKDS
181 LIDRRRTPGS SARSQKREAR LDKVLSDMKR HKKLEEQILR TGRDLFSLDS EDPSPASPPL
241 RSSGSSLFPR QRKYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PAGR1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.68
- Highest tissue expression
- 54 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 54 nTPM
- ovary: 33 nTPM
- pituitary gland: 23 nTPM
- cervix: 21 nTPM
- vagina: 15 nTPM
- endometrium: 14 nTPM
Single-cell type
- epicardial cells: 18 nCPM
- astrocytes: 2.2 nCPM
- ependymal cells: 2.2 nCPM
- bergmann glia: 1.6 nCPM
- brain excitatory neurons: 1.4 nCPM
- gastric chief cells: 1.1 nCPM
Immune cell
- eosinophil: 33 nTPM
- basophil: 23 nTPM
- MAIT T-cell: 22 nTPM
- naive CD4 T-cell: 22 nTPM
- plasmacytoid DC: 22 nTPM
- myeloid DC: 21 nTPM
Brain region
- cerebellum: 29 nTPM
- white matter: 16 nTPM
- cerebral cortex: 14 nTPM
- medulla oblongata: 14 nTPM
- midbrain: 13 nTPM
- pons: 13 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.54
- gnomAD pLI
- 0.74
- gnomAD missense Z
- 0.63
- DepMap mean gene effect
- -0.15
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA recombination
- DNA repair
- positive regulation of cell cycle G1/S phase transition
- positive regulation of intracellular estrogen receptor signaling pathway
- positive regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- PTIP-associated protein 1
- PAXIP1-associated-protein-1 C term PTIP binding protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PAGR1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PAGR1 as an antibody target. Whether an autoantibody or antibody against PAGR1 could matter depends on whether native PAGR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PAGR1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PAGR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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