UTP23
rRNA-processing protein UTP23 homolog
Also known as: C8orf53, MGC14595, UTP23_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BRU9
- Gene
- UTP23
- Ensembl
- ENSG00000147679
- Chromosome
- 8
- Canonical length
- 249 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoli
OverviewNCBI Gene
Enables mRNA 3'-UTR binding activity and mRNA 5'-UTR binding activity. Predicted to be involved in rRNA processing. Predicted to act upstream of or within endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Predicted to be located in nucleus. Predicted to be part of small-subunit processome. Predicted to be active in nucleolus. Implicated in colorectal adenocarcinoma. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
249 residues, UniProt reviewed canonical sequence.
>Q9BRU9|UTP23
1 MKITRQKHAK KHLGFFRNNF GVREPYQILL DGTFCQAALR GRIQLREQLP RYLMGETQLC
61 TTRCVLKELE TLGKDLYGAK LIAQKCQVRN CPHFKNAVSG SECLLSMVEE GNPHHYFVAT
121 QDQNLSVKVK KKPGVPLMFI IQNTMVLDKP SPKTIAFVKA VESGQLVSVH EKESIKHLKE
181 EQGLVKNTEQ SRRKKRKKIS GPNPLSCLKK KKKAPDTQSS ASEKKRKRKR IRNRSNPKVL
241 SEKQNAEGELocalizationUniProt · AlphaFold · HPA
Whether an antibody against UTP23 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)
- 0.41
- Highest tissue expression
- 12 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 12 nTPM
- ovary: 11 nTPM
- lymph node: 10 nTPM
- thyroid gland: 10 nTPM
- adipose tissue: 9.7 nTPM
- breast: 9 nTPM
Single-cell type
- brain inhibitory neurons: 90 nCPM
- brain excitatory neurons: 75 nCPM
- cardiomyocytes: 67 nCPM
- myonuclei: 61 nCPM
- retinal horizontal cells: 58 nCPM
- pancreatic acinar cells: 57 nCPM
Immune cell
- basophil: 50 nTPM
- naive CD4 T-cell: 48 nTPM
- T-reg: 44 nTPM
- memory B-cell: 44 nTPM
- naive B-cell: 42 nTPM
- gdT-cell: 40 nTPM
Brain region
- white matter: 14 nTPM
- cerebellum: 14 nTPM
- spinal cord: 13 nTPM
- basal ganglia: 12 nTPM
- hypothalamus: 12 nTPM
- cerebral cortex: 12 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)
- 0.9
- gnomAD pLI
- 0.09
- gnomAD missense Z
- 0.69
- DepMap mean gene effect
- -0.91
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 19% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- LSU-rRNA)
- endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA
- 5.8S rRNA
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Fcf1/UTP23
- PIN-like domain superfamily
- Fcf1
- UTP23, sensor motif region
- UTP23 sensor motif
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads UTP23 as an antibody target. Whether an autoantibody or antibody against UTP23 could matter depends on whether native UTP23 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
UTP23 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 UTP23 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...