ORM1
Alpha-1-acid glycoprotein 1
Also known as: A1AG1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P02763
- Gene
- ORM1
- Ensembl
- ENSG00000229314
- Chromosome
- 9
- Canonical length
- 201 aa
- Protein class
- Cancer-related genes, Candidate cardiovascular disease genes, FDA approved drug targets, Plasma proteins, Predicted secreted proteins
- Subcellular location
- Golgi apparatus,Vesicles
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This gene encodes a key acute phase plasma protein. Because of its increase due to acute inflammation, this protein is classified as an acute-phase reactant. The specific function of this protein has not yet been determined; however, it may be involved in aspects of immunosuppression. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
201 residues, UniProt reviewed canonical sequence.
>P02763|ORM1
1 MALSWVLTVL SLLPLLEAQI PLCANLVPVP ITNATLDRIT GKWFYIASAF RNEEYNKSVQ
61 EIQATFFYFT PNKTEDTIFL REYQTRQDQC IYNTTYLNVQ RENGTISRYV GGQEHFAHLL
121 ILRDTKTYML AFDVNDEKNW GLSVYADKPE TTKEQLGEFY EALDCLRIPK SDVVYTDWKK
181 DKCEPLEKQH EKERKQEEGE SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ORM1 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.33
- Highest tissue expression
- 42,168 nTPM
Expression across tissuesHPA
Tissue
- liver: 42,168 nTPM
- bone marrow: 226 nTPM
- prostate: 60 nTPM
- spleen: 47 nTPM
- lung: 27 nTPM
- stomach: 19 nTPM
Single-cell type
- hepatocytes: 63,161 nCPM
- cholangiocytes: 1,037 nCPM
- kupffer cells: 773 nCPM
- hepatic stellate cells: 387 nCPM
- neutrophils: 159 nCPM
- alveolar cells type 2: 75 nCPM
Immune cell
- neutrophil: 202 nTPM
- classical monocyte: 4.3 nTPM
- total PBMC: 1.9 nTPM
- non-classical monocyte: 1 nTPM
- intermediate monocyte: 0.5 nTPM
- basophil: 0 nTPM
Brain region
- medulla oblongata: 1 nTPM
- cerebral cortex: 0.9 nTPM
- basal ganglia: 0.7 nTPM
- choroid plexus: 0.6 nTPM
- hypothalamus: 0.6 nTPM
- spinal cord: 0.6 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)
- 1.29
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.34
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acute-phase response
- inflammatory response
- negative regulation of interleukin-6 production
- negative regulation of tumor necrosis factor production
- positive regulation of interleukin-1 beta production
- positive regulation of interleukin-1 production
- positive regulation of tumor necrosis factor production
- regulation of immune system process
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ORM1 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 ORM1 as an antibody target. Whether an autoantibody or antibody against ORM1 could matter depends on whether native ORM1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ORM1 is annotated as secreted, so native ORM1 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ORM1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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