TEDC1
Tubulin epsilon and delta complex protein 1
Also known as: C14orf80, TEDC1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86SX3
- Gene
- TEDC1
- Ensembl
- ENSG00000185347
- Chromosome
- 14
- Canonical length
- 495 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cytosol
OverviewNCBI Gene
Predicted to be involved in positive regulation of smoothened signaling pathway. Predicted to be located in centriole and cilium. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
495 residues, UniProt reviewed canonical sequence.
>Q86SX3|TEDC1
1 MGRRRQRVDP AAGARAGALP EAIAALSRSL PSGPSPEIFR RAKFDRPEAT SALWQLLFRV
61 LSPLPAGNAL ASLALEVQAR LVKSALCSQG YPRLALAQLP EDGSQGSREL LLALSWLLAR
121 GPVPEQMLAQ ARVPLGDEMT VCQCEALASP GPPAPHMEAE GPVDVRHVQW LMGKLRFRWR
181 QLVSSQQEQC ALLSKIHLYT RGCHSDQSLS HLSVTEAEML RDPEGGQQVS GAGAAQNLDL
241 AYPKCLHSFC TPGMGPRTFW NDLWLVCEQP GLLPGDWAAP LDPGGASACS LLSPFRALLR
301 TLERENQRLE AVLAWRRSEL VFWRWMDTVL GTCAPEVPAA ASQPTFLPWV PERGGGELDL
361 VVRELQALEE ELREAAERRR AAWEAKAGGC GRGPEWSAAR RASREAVEKE LGALQQCWER
421 DGGPAQPHGP HRLVRREDGA AGDRDLRAAV VIRTLRSQEA CLEAVLRRLQ GQCRQELARL
481 VGARPGLIWI PPPGRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TEDC1 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)
- 0.44
- Highest tissue expression
- 14 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 14 nTPM
- cerebral cortex: 13 nTPM
- amygdala: 13 nTPM
- hippocampal formation: 12 nTPM
- spinal cord: 9 nTPM
- midbrain: 8.9 nTPM
Single-cell type
- extravillous trophoblasts: 32 nCPM
- enteric transient amplifying cells: 29 nCPM
- colonocytes: 27 nCPM
- esophageal basal cells: 23 nCPM
- monocyte progenitors: 23 nCPM
- foveolar cells: 21 nCPM
Immune cell
- plasmacytoid DC: 2.4 nTPM
- memory CD8 T-cell: 1.4 nTPM
- intermediate monocyte: 0.9 nTPM
- memory CD4 T-cell: 0.8 nTPM
- non-classical monocyte: 0.8 nTPM
- myeloid DC: 0.7 nTPM
Brain region
- medulla oblongata: 18 nTPM
- cerebral cortex: 16 nTPM
- basal ganglia: 15 nTPM
- amygdala: 15 nTPM
- white matter: 15 nTPM
- hippocampal formation: 13 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)
- 0.7
- gnomAD pLI
- 0.01
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
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
- Tubulin epsilon and delta complex protein 1 domain
- Tubulin epsilon and delta complex protein 1
- Tubulin epsilon and delta complex protein 1
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TEDC1 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 TEDC1 as an antibody target. Whether an autoantibody or antibody against TEDC1 could matter depends on whether native TEDC1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TEDC1 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 TEDC1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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