CPSF4L
Putative cleavage and polyadenylation specificity factor subunit 4-like protein
Also known as: CPS4L_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- A6NMK7
- Gene
- CPSF4L
- Ensembl
- ENSG00000187959
- Chromosome
- 17
- Canonical length
- 179 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Predicted to enable RNA binding activity and zinc ion binding activity. Predicted to be involved in mRNA 3'-end processing. Predicted to be located in nucleus. Predicted to be part of mRNA cleavage and polyadenylation specificity factor complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
179 residues, UniProt reviewed canonical sequence.
>A6NMK7|CPSF4L
1 MQEVIAGLER FTFAFEKDVE MQKGTGLLPF QGMDKSASAV CNFFTKGLCE KGKLCPFRHD
61 RGEKMVVCKH WLRGLCKKGD HCKFLHQYDL TRMPECYFYS KFGDCSNKEC SFLHVKPAFK
121 SQDCPWYDQG FCKDGPLCKY RHVPRIMCLN YLVGFCPEGP KCQFAQKIRE FKLLPGSKILocalizationUniProt · AlphaFold · HPA
Whether an antibody against CPSF4L 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.45
- Highest tissue expression
- 0.6 nTPM
Expression across tissuesHPA
Tissue
- ovary: 0.6 nTPM
- retina: 0.5 nTPM
- salivary gland: 0.5 nTPM
- breast: 0.4 nTPM
- pancreas: 0.4 nTPM
- testis: 0.4 nTPM
Single-cell type
- oocytes: 32 nCPM
- salivary basal cells: 17 nCPM
- paneth cells: 7.7 nCPM
- pituicytes/fscs: 6.6 nCPM
- hepatic stellate cells: 6.5 nCPM
- müller glia: 6.3 nCPM
Immune cell
- eosinophil: 0.3 nTPM
- neutrophil: 0.1 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 2.9 nTPM
- medulla oblongata: 1.7 nTPM
- cerebral cortex: 1.3 nTPM
- midbrain: 1.3 nTPM
- white matter: 1.3 nTPM
- hippocampal formation: 1.2 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)
- 1.07
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.95
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CPSF4L as an antibody target. Whether an autoantibody or antibody against CPSF4L could matter depends on whether native CPSF4L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CPSF4L 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 CPSF4L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...