TPRKB
EKC/KEOPS complex subunit TPRKB
Also known as: CGI-121, CGI121, TPRKB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y3C4
- Gene
- TPRKB
- Ensembl
- ENSG00000144034
- Chromosome
- 2
- Canonical length
- 175 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Enables protein kinase binding activity. Involved in tRNA threonylcarbamoyladenosine modification. Located in cytosol and nucleus. Part of EKC/KEOPS complex. Implicated in Galloway-Mowat syndrome 5. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
175 residues, UniProt reviewed canonical sequence.
>Q9Y3C4|TPRKB
1 MQLTHQLDLF PECRVTLLLF KDVKNAGDLR RKAMEGTIDG SLINPTVIVD PFQILVAANK
61 AVHLYKLGKM KTRTLSTEII FNLSPNNNIS EALKKFGISA NDTSILIVYI EEGEKQINQE
121 YLISQVEGHQ VSLKNLPEIM NITEVKKIYK LSSQEESIGT LLDAIICRMS TKDVLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TPRKB 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)
- 0.27
- Highest tissue expression
- 67 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 67 nTPM
- bone marrow: 66 nTPM
- fallopian tube: 52 nTPM
- testis: 48 nTPM
- tongue: 48 nTPM
- ovary: 45 nTPM
Single-cell type
- late primary spermatocytes: 377 nCPM
- megakaryocytes: 216 nCPM
- epididymal efferent duct absorptive cells: 205 nCPM
- esophageal basal cells: 184 nCPM
- early primary spermatocytes: 181 nCPM
- esophageal apical cells: 168 nCPM
Immune cell
- basophil: 33 nTPM
- plasmacytoid DC: 30 nTPM
- eosinophil: 29 nTPM
- intermediate monocyte: 28 nTPM
- naive CD4 T-cell: 27 nTPM
- MAIT T-cell: 26 nTPM
Brain region
- cerebellum: 11 nTPM
- white matter: 8.4 nTPM
- cerebral cortex: 8.1 nTPM
- medulla oblongata: 7.8 nTPM
- pons: 7.5 nTPM
- spinal cord: 7.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TPRKB.
Disease | AllUniProt
Conditions TPRKB is implicated in, by any mechanism.
- Galloway-Mowat syndrome 5 (GAMOS5) MIM:617731
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 69 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Galloway-Mowat syndrome 5
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)
- 1.31
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- -0.59
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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
- CGI121/TPRKB
- CGI121/TPRKB superfamily
- Kinase binding protein CGI-121
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TPRKB 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 TPRKB as an antibody target. Whether an autoantibody or antibody against TPRKB could matter depends on whether native TPRKB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TPRKB 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 TPRKB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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