TSACC
TSSK6-activating co-chaperone protein
Also known as: C1orf182, SIP, SSTK-IP, TSACC_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96A04
- Gene
- TSACC
- Ensembl
- ENSG00000163467
- Chromosome
- 1
- Canonical length
- 125 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
Enables protein-folding chaperone binding activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
125 residues, UniProt reviewed canonical sequence.
>Q96A04|TSACC
1 MERHTSHPNR KVPAKEEANA VPLCRAKPSP SYINLQASSP PATFLNIQTT KLPSVDHKPK
61 ECLGLLECMY ANLQLQTQLA QQQMAVLEHL QASVTQLAPG RGSNNSSLPA LSPNPLLNHL
121 PQFSKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TSACC 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)
- 0.63
- Highest tissue expression
- 879 nTPM
Expression across tissuesHPA
Tissue
- testis: 879 nTPM
- epididymis: 2.3 nTPM
- retina: 2.1 nTPM
- liver: 1.7 nTPM
- adrenal gland: 1.4 nTPM
- spinal cord: 1.3 nTPM
Single-cell type
- late spermatids: 29,125 nCPM
- late primary spermatocytes: 7,373 nCPM
- early spermatids: 6,461 nCPM
- early primary spermatocytes: 328 nCPM
- cardiomyocytes: 107 nCPM
- sertoli cells: 57 nCPM
Immune cell
- basophil: 15 nTPM
- NK-cell: 1.9 nTPM
- plasmacytoid DC: 1.7 nTPM
- naive CD4 T-cell: 1.5 nTPM
- naive B-cell: 1.4 nTPM
- naive CD8 T-cell: 1.3 nTPM
Brain region
- white matter: 8 nTPM
- cerebellum: 6.2 nTPM
- choroid plexus: 5.4 nTPM
- medulla oblongata: 5.2 nTPM
- pons: 5.2 nTPM
- basal ganglia: 5.1 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)
- 1.53
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- -0.26
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- TSSK6-activating co-chaperone protein
- SSTK-interacting protein, TSSK6-activating co-chaperone protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TSACC in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
- HSP70
- TSSK6
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TSACC as an antibody target. Whether an autoantibody or antibody against TSACC could matter depends on whether native TSACC is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TSACC 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 TSACC as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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