EBAG9
Receptor-binding cancer antigen expressed on SiSo cells
Also known as: EB9, RCAS1, RCAS1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00559
- Gene
- EBAG9
- Ensembl
- ENSG00000147654
- Chromosome
- 8
- Canonical length
- 213 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins
- Subcellular location
- Golgi apparatus
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene was identified as an estrogen-responsive gene. Regulation of transcription by estrogen is mediated by estrogen receptor, which binds to the estrogen-responsive element found in the 5'-flanking region of this gene. The encoded protein is a tumor-associated antigen that is expressed at high frequency in a variety of cancers. Alternate splicing results in multiple transcript variants. A pseudogene of this gene has been defined on chromosome 10. [provided by RefSeq, Jul 2013]
Canonical amino-acid sequenceUniProt
213 residues, UniProt reviewed canonical sequence.
>O00559|EBAG9
1 MAITQFRLFK FCTCLATVFS FLKRLICRSG RGRKLSGDQI TLPTTVDYSS VPKQTDVEEW
61 TSWDEDAPTS VKIEGGNGNV ATQQNSLEQL EPDYFKDMTP TIRKTQKIVI KKREPLNFGI
121 PDGSTGFSSR LAATQDLPFI HQSSELGDLD TWQENTNAWE EEEDAAWQAE EVLRQQKLAD
181 REKRAAEQQR KKMEKEAQRL MKKEQNKIGV KLSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against EBAG9 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.64
- Highest tissue expression
- 50 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 50 nTPM
- skeletal muscle: 44 nTPM
- epididymis: 38 nTPM
- salivary gland: 37 nTPM
- tongue: 37 nTPM
- liver: 36 nTPM
Single-cell type
- late spermatids: 172 nCPM
- late primary spermatocytes: 145 nCPM
- early spermatids: 119 nCPM
- epididymal principal cells: 106 nCPM
- early primary spermatocytes: 93 nCPM
- gastric chief cells: 93 nCPM
Immune cell
- memory B-cell: 29 nTPM
- naive B-cell: 29 nTPM
- MAIT T-cell: 24 nTPM
- naive CD4 T-cell: 23 nTPM
- T-reg: 22 nTPM
- NK-cell: 21 nTPM
Brain region
- cerebellum: 29 nTPM
- cerebral cortex: 25 nTPM
- hypothalamus: 24 nTPM
- basal ganglia: 23 nTPM
- white matter: 22 nTPM
- medulla oblongata: 22 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)
- 0.73
- gnomAD pLI
- 0.08
- gnomAD missense Z
- 0.97
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 17% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune memory response involving T cells and B cells
- regulation of cell growth
- T cell mediated cytotoxicity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cancer-associated antigen RCAS1
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads EBAG9 as an antibody target. Whether an autoantibody or antibody against EBAG9 could matter depends on whether native EBAG9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
EBAG9 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 EBAG9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...