TCEANC
Transcription elongation factor A N-terminal and central domain-containing protein
Also known as: MGC17403, TEANC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N8B7
- Gene
- TCEANC
- Ensembl
- ENSG00000176896
- Chromosome
- X
- Canonical length
- 351 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nuclear speckles
OverviewNCBI Gene
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
351 residues, UniProt reviewed canonical sequence.
>Q8N8B7|TCEANC
1 MSDKNQIAAR ASLIEQLMSK RNFEDLGNHL TELETIYVTK EHLQETDVVR AVYRVLKNCP
61 SVALKKKAKC LLSKWKAVYK QTHSKARNSP KLFPVRGNKE ENSGPSHDPS QNETLGICSS
121 NSLSSQDVAK LSEMIVPENR AIQLKPKEEH FGDGDPESTG KRSSELLDPT TPMRTKCIEL
181 LYAALTSSST DQPKADLWQN FAREIEEHVF TLYSKNIKKY KTCIRSKVAN LKNPRNSHLQ
241 QNLLSGTTSP REFAEMTVME MANKELKQLR ASYTESCIQE HYLPQVIDGT QTNKIKCRRC
301 EKYNCKVTVI DRGTLFLPSW VRNSNPDEQM MTYVICNECG EQWYHSKWVC WLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TCEANC 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)
- 0.43
- Highest tissue expression
- 5.3 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 5.3 nTPM
- retina: 3.5 nTPM
- thymus: 3.1 nTPM
- lymph node: 3 nTPM
- ovary: 2.9 nTPM
- spleen: 2.8 nTPM
Single-cell type
- myonuclei: 16 nCPM
- plasma cells: 12 nCPM
- retinal horizontal cells: 10 nCPM
- neutrophils: 9.6 nCPM
- erythrocytes: 9 nCPM
- b-cells: 8.4 nCPM
Immune cell
- basophil: 11 nTPM
- eosinophil: 7.8 nTPM
- T-reg: 6.6 nTPM
- naive CD4 T-cell: 6.5 nTPM
- memory B-cell: 6.4 nTPM
- naive B-cell: 6.1 nTPM
Brain region
- cerebellum: 5.5 nTPM
- white matter: 5.4 nTPM
- pons: 4.3 nTPM
- spinal cord: 4.2 nTPM
- basal ganglia: 4.1 nTPM
- cerebral cortex: 4.1 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)
- 1.07
- gnomAD pLI
- 0.05
- gnomAD missense Z
- 0.28
- DepMap mean gene effect
- 0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Transcription elongation factor S-II, central domain
- 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), central domain
- TFIIS helical bundle-like domain
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TCEANC as an antibody target. Whether an autoantibody or antibody against TCEANC could matter depends on whether native TCEANC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TCEANC 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 TCEANC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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