THOC3
THO complex subunit 3
Also known as: MGC5469, TEX1, THOC3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96J01
- Gene
- THOC3
- Ensembl
- ENSG00000051596
- Chromosome
- 5
- Canonical length
- 351 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Vesicles
OverviewNCBI Gene
This gene encodes a component of the nuclear THO transcription elongation complex, which is part of the larger transcription export (TREX) complex that couples messenger RNA processing and export. In humans, the transcription export complex is recruited to the 5'-end of messenger RNAs in a splicing- and cap-dependent manner. Studies of a related complex in mouse suggest that the metazoan transcription export complex is involved in cell differentiation and development. A pseudogene of this gene has been defined on chromosome 5. [provided by RefSeq, May 2013]
Canonical amino-acid sequenceUniProt
351 residues, UniProt reviewed canonical sequence.
>Q96J01|THOC3
1 MAVPAAAMGP SALGQSGPGS MAPWCSVSSG PSRYVLGMQE LFRGHSKTRE FLAHSAKVHS
61 VAWSCDGRRL ASGSFDKTAS VFLLEKDRLV KENNYRGHGD SVDQLCWHPS NPDLFVTASG
121 DKTIRIWDVR TTKCIATVNT KGENINICWS PDGQTIAVGN KDDVVTFIDA KTHRSKAEEQ
181 FKFEVNEISW NNDNNMFFLT NGNGCINILS YPELKPVQSI NAHPSNCICI KFDPMGKYFA
241 TGSADALVSL WDVDELVCVR CFSRLDWPVR TLSFSHDGKM LASASEDHFI DIAEVETGDK
301 LWEVQCESPT FTVAWHPKRP LLAFACDDKD GKYDSSREAG TVKLFGLPND SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against THOC3 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)
- 0.26
- Highest tissue expression
- 101 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 101 nTPM
- esophagus: 80 nTPM
- tonsil: 67 nTPM
- bone marrow: 55 nTPM
- choroid plexus: 50 nTPM
- testis: 49 nTPM
Single-cell type
- papillary tip epithelial cells: 112 nCPM
- early spermatids: 106 nCPM
- renal connecting tubule cells: 62 nCPM
- late primary spermatocytes: 62 nCPM
- late spermatids: 60 nCPM
- esophageal apical cells: 43 nCPM
Immune cell
- T-reg: 199 nTPM
- naive CD4 T-cell: 152 nTPM
- memory CD4 T-cell: 124 nTPM
- naive B-cell: 111 nTPM
- naive CD8 T-cell: 93 nTPM
- total PBMC: 83 nTPM
Brain region
- cerebral cortex: 128 nTPM
- hippocampal formation: 122 nTPM
- cerebellum: 65 nTPM
- amygdala: 62 nTPM
- choroid plexus: 45 nTPM
- white matter: 39 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)
- 0.93
- gnomAD pLI
- 0.03
- gnomAD missense Z
- 2.05
- DepMap mean gene effect
- -1.3
- DepMap dependency class
- common
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- WD40 repeat
- WD40/YVTN repeat-like-containing domain superfamily
- PAC1/LIS1-like, WD-40 repeat
- WD40-repeat-containing domain superfamily
- TREX component Tex1/THOC3
- THOC3 beta-propeller domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of THOC3 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 THOC3 as an antibody target. Whether an autoantibody or antibody against THOC3 could matter depends on whether native THOC3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
THOC3 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 THOC3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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