TCEA3
Transcription elongation factor A protein 3
Also known as: TCEA3_HUMAN, TFIIS.H
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O75764
- Gene
- TCEA3
- Ensembl
- ENSG00000204219
- Chromosome
- 1
- Canonical length
- 348 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
Predicted to enable DNA binding activity; translation elongation factor activity; and zinc ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
348 residues, UniProt reviewed canonical sequence.
>O75764|TCEA3
1 MGQEEELLRI AKKLEKMVAR KNTEGALDLL KKLHSCQMSI QLLQTTRIGV AVNGVRKHCS
61 DKEVVSLAKV LIKNWKRLLD SPGPPKGEKG EEREKAKKKE KGLECSDWKP EAGLSPPRKK
121 REDPKTRRDS VDSKSSASSS PKRPSVERSN SSKSKAESPK TPSSPLTPTF ASSMCLLAPC
181 YLTGDSVRDK CVEMLSAALK ADDDYKDYGV NCDKMASEIE DHIYQELKST DMKYRNRVRS
241 RISNLKDPRN PGLRRNVLSG AISAGLIAKM TAEEMASDEL RELRNAMTQE AIREHQMAKT
301 GGTTTDLFQC SKCKKKNCTY NQVQTRSADE PMTTFVLCNE CGNRWKFCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TCEA3 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)
- 0.45
- Highest tissue expression
- 446 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 446 nTPM
- pancreas: 190 nTPM
- tongue: 162 nTPM
- liver: 133 nTPM
- salivary gland: 83 nTPM
- adrenal gland: 79 nTPM
Single-cell type
- goblet cells: 274 nCPM
- gastric progenitor cells: 179 nCPM
- enteric transient amplifying cells: 169 nCPM
- hepatocytes: 168 nCPM
- colonocytes: 167 nCPM
- granulosa cells: 157 nCPM
Immune cell
- naive CD4 T-cell: 14 nTPM
- memory CD4 T-cell: 8.4 nTPM
- naive CD8 T-cell: 6.1 nTPM
- myeloid DC: 2.9 nTPM
- total PBMC: 2.3 nTPM
- memory CD8 T-cell: 1.1 nTPM
Brain region
- choroid plexus: 12 nTPM
- medulla oblongata: 8.4 nTPM
- spinal cord: 6.5 nTPM
- white matter: 6.1 nTPM
- cerebral cortex: 6 nTPM
- midbrain: 5.9 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
- gnomAD missense Z
- 0.95
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Zinc finger, TFIIS-type
- Transcription elongation factor, TFIIS/CRSP70, N-terminal, sub-type
- Transcription elongation factor S-II, central domain
- Transcription elongation factor, TFIIS
- Transcription factor IIS, N-terminal
- Transcription elongation factor, IIS-type
- TFIIS/LEDGF domain superfamily
- Transcription elongation factor S-II, central domain superfamily
- Transcription factor S-II (TFIIS)
- Transcription factor S-II (TFIIS), central domain
- TFIIS helical bundle-like domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TCEA3 as an antibody target. Whether an autoantibody or antibody against TCEA3 could matter depends on whether native TCEA3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TCEA3 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 TCEA3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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