CCDC59
Thyroid transcription factor 1-associated protein 26
Also known as: BR22, HSPC128, TAP26, TAP26_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P031
- Gene
- CCDC59
- Ensembl
- ENSG00000133773
- Chromosome
- 12
- Canonical length
- 241 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli,Nucleoli rim,Plasma membrane
OverviewNCBI Gene
Enables RNA binding activity. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
241 residues, UniProt reviewed canonical sequence.
>Q9P031|CCDC59
1 MAPVRRSAKW RPGGIEARGE GVSTVGYRNK NVRQKTWRPN HPQAFVGSVR EGQGFAFRRK
61 LKIQQSYKKL LRKEKKAQTS LESQFTDRYP DNLKHLYLAE EERHRKQARK VDHPLSEQVH
121 QPLLEEQCSI DEPLFEDQCS FDQPQPEEQC IKTVNSFTIP KKNKKKTSNQ KAQEEYEQIQ
181 AKRAAKKQEF ERRKQEREEA QRQYKKKKME VFKILNKKTK KGQPNLNVQM EYLLQKIQEK
241 CLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCDC59 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)
- 0.59
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 38 nTPM
- tongue: 18 nTPM
- skeletal muscle: 15 nTPM
- choroid plexus: 13 nTPM
- adipose tissue: 13 nTPM
- blood vessel: 12 nTPM
Single-cell type
- oocytes: 332 nCPM
- late primary spermatocytes: 310 nCPM
- cardiomyocytes: 229 nCPM
- syncytiotrophoblasts: 186 nCPM
- early primary spermatocytes: 166 nCPM
- epididymal principal cells: 154 nCPM
Immune cell
- T-reg: 30 nTPM
- basophil: 26 nTPM
- naive B-cell: 24 nTPM
- neutrophil: 23 nTPM
- naive CD4 T-cell: 22 nTPM
- MAIT T-cell: 22 nTPM
Brain region
- white matter: 19 nTPM
- cerebral cortex: 16 nTPM
- cerebellum: 14 nTPM
- medulla oblongata: 14 nTPM
- basal ganglia: 13 nTPM
- amygdala: 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)
- 1.7
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.37
- DepMap mean gene effect
- -0.61
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Fyv7/TAP26
- rRNA processing
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCDC59 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 CCDC59 as an antibody target. Whether an autoantibody or antibody against CCDC59 could matter depends on whether native CCDC59 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCDC59 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 CCDC59 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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