CCNL1
Cyclin-L1
Also known as: ania-6a, CCNL1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9UK58
- Gene
- CCNL1
- Ensembl
- ENSG00000163660
- Chromosome
- 3
- Canonical length
- 526 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nuclear bodies
OverviewNCBI Gene
Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Involved in regulation of RNA splicing. Located in nucleus. Part of cyclin-dependent protein kinase holoenzyme complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
526 residues, UniProt reviewed canonical sequence.
>Q9UK58|CCNL1
1 MASGPHSTAT AAAAASSAAP SAGGSSSGTT TTTTTTTGGI LIGDRLYSEV SLTIDHSLIP
61 EERLSPTPSM QDGLDLPSET DLRILGCELI QAAGILLRLP QVAMATGQVL FHRFFYSKSF
121 VKHSFEIVAM ACINLASKIE EAPRRIRDVI NVFHHLRQLR GKRTPSPLIL DQNYINTKNQ
181 VIKAERRVLK ELGFCVHVKH PHKIIVMYLQ VLECERNQTL VQTAWNYMND SLRTNVFVRF
241 QPETIACACI YLAARALQIP LPTRPHWFLL FGTTEEEIQE ICIETLRLYT RKKPNYELLE
301 KEVEKRKVAL QEAKLKAKGL NPDGTPALST LGGFSPASKP SSPREVKAEE KSPISINVKT
361 VKKEPEDRQQ ASKSPYNGVR KDSKRSRNSR SASRSRSRTR SRSRSHTPRR HYNNRRSRSG
421 TYSSRSRSRS RSHSESPRRH HNHGSPHLKA KHTRDDLKSS NRHGHKRKKS RSRSQSKSRD
481 HSDAAKKHRH ERGHHRDRRE RSRSFERSHK SKHHGGSRSG HGRHRRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCNL1 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)
- 0.49
- Highest tissue expression
- 56 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 56 nTPM
- bone marrow: 53 nTPM
- liver: 48 nTPM
- spleen: 40 nTPM
- pancreas: 35 nTPM
- ovary: 33 nTPM
Single-cell type
- neutrophils: 1,427 nCPM
- endometrial glandular cells: 874 nCPM
- endometrial luminal cells: 865 nCPM
- neutrophil progenitors: 609 nCPM
- epididymal basal cells: 557 nCPM
- salivary myoepithelial cells: 544 nCPM
Immune cell
- neutrophil: 29 nTPM
- NK-cell: 17 nTPM
- naive CD4 T-cell: 17 nTPM
- eosinophil: 16 nTPM
- T-reg: 15 nTPM
- naive B-cell: 15 nTPM
Brain region
- medulla oblongata: 16 nTPM
- cerebral cortex: 15 nTPM
- white matter: 14 nTPM
- cerebellum: 14 nTPM
- hypothalamus: 12 nTPM
- thalamus: 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)
- 0.26
- gnomAD pLI
- 1
- gnomAD missense Z
- 2.6
- DepMap mean gene effect
- -0.57
- DepMap dependency class
- common
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
- regulation of apoptotic process
- regulation of cell cycle
- regulation of centrosome cycle
- regulation of RNA splicing
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCNL1 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 CCNL1 as an antibody target. Whether an autoantibody or antibody against CCNL1 could matter depends on whether native CCNL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCNL1 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 CCNL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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