TRGC1
T cell receptor gamma constant 1
Also known as: TRGC1_HUMAN
Protein identityUniProt · HPA
- UniProt accession
- P0CF51
- Gene
- TRGC1
- Canonical length
- 173 aa
- Protein class
- Predicted membrane proteins, T-cell receptor genes
- Quaternary structure
- Homodimer
OverviewNCBI Gene
No narrative summary is available for TRGC1 in this catalog release; identity and structured annotations are shown without generated factual claims.
Canonical amino-acid sequenceUniProt
173 residues, UniProt reviewed canonical sequence.
>P0CF51|TRGC1
1 DKQLDADVSP KPTIFLPSIA ETKLQKAGTY LCLLEKFFPD VIKIHWQEKK SNTILGSQEG
61 NTMKTNDTYM KFSWLTVPEK SLDKEHRCIV RHENNKNGVD QEIIFPPIKT DVITMDPKDN
121 CSKDANDTLL LQLTNTSAYY MYLLLLLKSV VYFAIITCCL LRRTAFCCNG EKSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRGC1 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 0
- Highest tissue expression
- 39 nTPM
Expression across tissuesHPA
Tissue
- prostate: 39 nTPM
- bone marrow: 18 nTPM
- spleen: 3.6 nTPM
- thymus: 3 nTPM
- lung: 1.7 nTPM
- midbrain: 1.4 nTPM
Single-cell type
- nk-cells: 17 nCPM
- prostatic glandular cells: 16 nCPM
- innate lymphoid cells: 8.6 nCPM
- renal collecting duct intercalated cells: 8.6 nCPM
- t-cells: 7.4 nCPM
- neutrophil progenitors: 6.2 nCPM
Immune cell
- gdT-cell: 60 nTPM
- NK-cell: 18 nTPM
- MAIT T-cell: 11 nTPM
- memory CD8 T-cell: 5.2 nTPM
- total PBMC: 4.7 nTPM
- basophil: 3.2 nTPM
Brain region
- thalamus: 1.3 nTPM
- pons: 1 nTPM
- amygdala: 0.8 nTPM
- medulla oblongata: 0.8 nTPM
- basal ganglia: 0.7 nTPM
- midbrain: 0.7 nTPM
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TRGC1 as an antibody target. Whether an autoantibody or antibody against TRGC1 could matter depends on whether native TRGC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRGC1 is annotated at the cell surface, where native TRGC1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label TRGC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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