CHTF8
Chromosome transmission fidelity protein 8 homolog
Also known as: CTF8, CTF8_HUMAN, FLJ20400
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P0CG13
- Gene
- CHTF8
- Ensembl
- ENSG00000168802
- Chromosome
- 16
- Canonical length
- 121 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a short protein that forms part of the Ctf18 replication factor C (RFC) complex that occurs in both yeast and mammals. The heteroheptameric RFC complex plays a role in sister chromatid cohesion and may load the replication clamp PCNA (proliferating cell nuclear antigen) onto DNA during DNA replication and repair. This gene is ubiquitously expressed and has been shown to have reduced expression in renal and prostate tumors. Alternatively spliced transcript variants have been described. This gene has a pseudogene on chromosome X. [provided by RefSeq, Oct 2018]
Canonical amino-acid sequenceUniProt
121 residues, UniProt reviewed canonical sequence.
>P0CG13|CHTF8
1 MVQIVISSAR AGGLAEWVLM ELQGEIEARY STGLAGNLLG DLHYTTEGIP VLIVGHHILY
61 GKIIHLEKPF AVLVKHTPGD QDCDELGRET GTRYLVTALI KDKILFKTRP KPIITSVPKK
121 VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CHTF8 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
- 67 nTPM
Expression across tissuesHPA
Tissue
- kidney: 67 nTPM
- liver: 66 nTPM
- pancreas: 47 nTPM
- spleen: 43 nTPM
- stomach: 43 nTPM
- esophagus: 41 nTPM
Single-cell type
- proximal tubule cells: 47 nCPM
- choroid plexus epithelial cells: 40 nCPM
- podocytes: 31 nCPM
- renal collecting duct intercalated cells: 25 nCPM
- distal convoluted tubule cells: 24 nCPM
- loop of henle epithelial cells: 24 nCPM
Immune cell
- basophil: 69 nTPM
- non-classical monocyte: 39 nTPM
- total PBMC: 39 nTPM
- naive B-cell: 36 nTPM
- classical monocyte: 35 nTPM
- intermediate monocyte: 35 nTPM
Brain region
- choroid plexus: 26 nTPM
- white matter: 19 nTPM
- basal ganglia: 19 nTPM
- hippocampal formation: 18 nTPM
- cerebral cortex: 18 nTPM
- hypothalamus: 15 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)
- 0.51
- gnomAD pLI
- 0.83
- gnomAD missense Z
- 0.95
- DepMap mean gene effect
- -0.41
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA replication
- mitotic sister chromatid cohesion
- positive regulation of DNA-directed DNA polymerase activity
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Chromosome transmission fidelity protein 8
- Ctf8
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CHTF8 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 CHTF8 as an antibody target. Whether an autoantibody or antibody against CHTF8 could matter depends on whether native CHTF8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CHTF8 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 CHTF8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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