CCNP
gene geneOn this page
Also known as FLJ13265
Summary
CCNP (cyclin P, HGNC:25805) is a protein-coding gene on chromosome 19q13.2, encoding Cyclin-P (Q9H8S5). Seems to be involved in the regulation of proliferation and migration.
Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Predicted to be involved in G1/S transition of mitotic cell cycle. Located in nucleus.
Source: NCBI Gene 79935 — RefSeq curated summary.
At a glance
- Clinical variants (ClinVar): 58 total
- MANE Select transcript:
NM_024877
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:25805 |
| Approved symbol | CCNP |
| Name | cyclin P |
| Location | 19q13.2 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | FLJ13265 |
| Ensembl gene | ENSG00000105219 |
| Ensembl biotype | protein_coding |
| OMIM | 620396 |
| Entrez | 79935 |
Gene structure
Transcript identifiers
Ensembl transcripts: 7 — 5 protein_coding, 1 nonsense_mediated_decay, 1 retained_intron
ENST00000221818, ENST00000430325, ENST00000513948, ENST00000593335, ENST00000599263, ENST00000921917, ENST00000921918
RefSeq mRNA: 2 — MANE Select: NM_024877
NM_001411133, NM_024877
CCDS: CCDS12551, CCDS92618
Canonical transcript exons
ENST00000430325 — 5 exons
| Exon | Start | End |
|---|---|---|
| ENSE00000706480 | 40224488 | 40224643 |
| ENSE00001641476 | 40226375 | 40226689 |
| ENSE00001644028 | 40224722 | 40224811 |
| ENSE00001788472 | 40223388 | 40223546 |
| ENSE00002028229 | 40222208 | 40223303 |
Expression profiles
Bgee: expression breadth ubiquitous, 153 present calls, max score 98.38.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.2303 / max 17.6767, expressed in 88 samples.
FANTOM5 promoters (3 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 180951 | 0.1830 | 75 |
| 180950 | 0.0347 | 8 |
| 180949 | 0.0126 | 3 |
Top tissues by expression
281 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 98.38 | gold quality |
| oocyte | CL:0000023 | 89.51 | gold quality |
| pancreatic ductal cell | CL:0002079 | 86.25 | silver quality |
| right hemisphere of cerebellum | UBERON:0014890 | 85.85 | gold quality |
| cerebellar hemisphere | UBERON:0002245 | 85.81 | gold quality |
| cerebellar cortex | UBERON:0002129 | 85.57 | gold quality |
| cerebellum | UBERON:0002037 | 83.56 | gold quality |
| type B pancreatic cell | CL:0000169 | 81.34 | gold quality |
| olfactory bulb | UBERON:0002264 | 81.30 | gold quality |
| secondary oocyte | CL:0000655 | 81.26 | gold quality |
| metanephros cortex | UBERON:0010533 | 80.99 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 79.12 | gold quality |
| tibialis anterior | UBERON:0001385 | 78.75 | silver quality |
| superficial temporal artery | UBERON:0001614 | 75.18 | gold quality |
| right lobe of liver | UBERON:0001114 | 74.35 | gold quality |
| orbitofrontal cortex | UBERON:0004167 | 74.16 | gold quality |
| ileal mucosa | UBERON:0000331 | 72.68 | silver quality |
| pituitary gland | UBERON:0000007 | 71.55 | gold quality |
| triceps brachii | UBERON:0001509 | 71.07 | gold quality |
| right uterine tube | UBERON:0001302 | 71.03 | gold quality |
| vastus lateralis | UBERON:0001379 | 71.02 | gold quality |
| biceps brachii | UBERON:0001507 | 71.02 | gold quality |
| CA1 field of hippocampus | UBERON:0003881 | 71.02 | gold quality |
| adenohypophysis | UBERON:0002196 | 70.04 | gold quality |
| metanephros | UBERON:0000081 | 69.61 | gold quality |
| gluteal muscle | UBERON:0002000 | 69.59 | gold quality |
| tongue squamous epithelium | UBERON:0006919 | 69.45 | gold quality |
| upper arm skin | UBERON:0004263 | 69.40 | gold quality |
| parotid gland | UBERON:0001831 | 69.08 | gold quality |
| myocardium | UBERON:0002349 | 67.78 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 1.27 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
36 targeting CCNP, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-4534 | 99.99 | 66.58 | 1907 |
| HSA-MIR-4531 | 99.99 | 69.70 | 3181 |
| HSA-MIR-605-3P | 99.88 | 69.22 | 1833 |
| HSA-MIR-4728-5P | 99.85 | 69.39 | 4718 |
| HSA-MIR-6785-5P | 99.82 | 68.68 | 4428 |
| HSA-MIR-149-3P | 99.72 | 68.22 | 3963 |
| HSA-MIR-6883-5P | 99.69 | 68.05 | 3785 |
| HSA-MIR-646 | 99.68 | 67.84 | 1645 |
| HSA-MIR-4441 | 99.49 | 66.56 | 3216 |
| HSA-MIR-3915 | 99.45 | 68.49 | 1905 |
| HSA-MIR-3960 | 99.41 | 66.11 | 96 |
| HSA-MIR-584-3P | 99.35 | 67.69 | 1082 |
| HSA-MIR-532-3P | 99.34 | 65.76 | 1195 |
| HSA-MIR-422A | 99.18 | 65.83 | 550 |
| HSA-MIR-6809-5P | 99.13 | 68.45 | 1223 |
| HSA-MIR-7160-5P | 99.11 | 67.17 | 2207 |
| HSA-MIR-4478 | 99.07 | 65.16 | 2320 |
| HSA-MIR-4270 | 99.02 | 66.26 | 1987 |
| HSA-MIR-6754-5P | 98.60 | 65.54 | 1627 |
| HSA-MIR-4463 | 98.56 | 66.05 | 1071 |
| HSA-MIR-378A-3P | 98.43 | 66.10 | 548 |
| HSA-MIR-378B | 98.43 | 65.36 | 573 |
| HSA-MIR-378C | 98.43 | 66.10 | 548 |
| HSA-MIR-378D | 98.43 | 66.10 | 548 |
| HSA-MIR-378E | 98.43 | 65.99 | 551 |
| HSA-MIR-378F | 98.43 | 65.66 | 554 |
| HSA-MIR-378H | 98.43 | 66.16 | 545 |
| HSA-MIR-378I | 98.43 | 66.10 | 548 |
| HSA-MIR-758-3P | 98.42 | 68.60 | 1122 |
| HSA-MIR-8072 | 98.27 | 66.24 | 83 |
Literature-anchored findings (GeneRIF, showing 3)
- Study reports that CNTD2 is upregulated in human lung cancer tissues and correlates with worse prognosis. CNTD2 is found to be an oncogenic driver in lung cancer cell lines and mouse xenograft models. (PMID:28860486)
- CNTD2 is significantly upregulated in Colorectal cancer (CRC) tissue compared to the adjacent normal one. CNTD2 overexpression in CRC cell lines increases their proliferation capacity and migration, as well as spheroid formation capacity and anchorage-independent growth. (PMID:30087414)
- Atypical cyclin P regulates cancer cell stemness through activation of the WNT pathway. (PMID:34604945)
Cross-species orthologs
9 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| danio_rerio | ccnp | ENSDARG00000055250 |
| drosophila_melanogaster | CycB | FBGN0000405 |
| drosophila_melanogaster | CycD | FBGN0010315 |
| drosophila_melanogaster | CycE | FBGN0010382 |
| caenorhabditis_elegans | WBGENE00000865 | |
| caenorhabditis_elegans | WBGENE00000866 | |
| caenorhabditis_elegans | cyb-2.2 | WBGENE00000867 |
| caenorhabditis_elegans | WBGENE00000870 | |
| caenorhabditis_elegans | cye-1 | WBGENE00000871 |
Paralogs (18): CCNE1 (ENSG00000105173), CCNJ (ENSG00000107443), CCND1 (ENSG00000110092), CCND3 (ENSG00000112576), CCNG1 (ENSG00000113328), CCNI (ENSG00000118816), CCND2 (ENSG00000118971), CCNA1 (ENSG00000133101), CCNB1 (ENSG00000134057), CCNJL (ENSG00000135083), CCNG2 (ENSG00000138764), CCNA2 (ENSG00000145386), CCNB3 (ENSG00000147082), CCNO (ENSG00000152669), CCNB2 (ENSG00000157456), CCNF (ENSG00000162063), CCNE2 (ENSG00000175305), CCNI2 (ENSG00000205089)
Protein
Protein identifiers
Cyclin-P — Q9H8S5 (reviewed: Q9H8S5)
Alternative names: Cyclin N-terminal domain-containing protein 2
All UniProt accessions (3): Q9H8S5, D6RCS3, M0QZM5
UniProt curated annotations — full annotation on UniProt →
Function. Seems to be involved in the regulation of proliferation and migration.
Subcellular location. Nucleus.
Tissue specificity. Expression is induced in lung and colon cancer cells.
Miscellaneous. May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay.
Isoforms (2)
| UniProt ID | Names | Canonical? |
|---|---|---|
| Q9H8S5-1 | 1 | yes |
| Q9H8S5-2 | 2 |
RefSeq proteins (2): NP_001398062, NP_079153* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR006671 | Cyclin_N | Domain |
| IPR013763 | Cyclin-like_dom | Domain |
| IPR036915 | Cyclin-like_sf | Homologous_superfamily |
| IPR039361 | Cyclin | Family |
Pfam: PF00134
UniProt features (7 total): splice variant 3, region of interest 2, chain 1, domain 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q9H8S5-F1 | 70.87 | 0.38 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 43 (showing top):
GSE45365_CD8A_DC_VS_CD11B_DC_IFNAR_KO_MCMV_INFECTION_DN, GOBP_CELL_CYCLE_PHASE_TRANSITION, GOBP_CELL_CYCLE_G1_S_PHASE_TRANSITION, GOBP_MITOTIC_CELL_CYCLE, KUUSELO_PANCREATIC_CANCER_19Q13_AMPLIFICATION, GOCC_TRANSFERASE_COMPLEX_TRANSFERRING_PHOSPHORUS_CONTAINING_GROUPS, GOCC_TRANSFERASE_COMPLEX, GOCC_PROTEIN_KINASE_COMPLEX, GOBP_CELL_CYCLE_PROCESS, GOCC_CYCLIN_DEPENDENT_PROTEIN_KINASE_HOLOENZYME_COMPLEX, GOMF_ENZYME_REGULATOR_ACTIVITY, MOREAUX_MULTIPLE_MYELOMA_BY_TACI_UP, BHAT_ESR1_TARGETS_VIA_AKT1_UP, ZWANG_TRANSIENTLY_UP_BY_2ND_EGF_PULSE_ONLY, PTEN_DN.V1_UP
GO Biological Process (1): G1/S transition of mitotic cell cycle (GO:0000082)
GO Molecular Function (1): cyclin-dependent protein serine/threonine kinase regulator activity (GO:0016538)
GO Cellular Component (3): cyclin-dependent protein kinase holoenzyme complex (GO:0000307), nucleus (GO:0005634), cytoplasm (GO:0005737)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| mitotic cell cycle | 1 |
| mitotic cell cycle phase transition | 1 |
| cell cycle G1/S phase transition | 1 |
| cyclin-dependent protein serine/threonine kinase activity | 1 |
| cyclin-dependent protein kinase regulator activity | 1 |
| serine/threonine protein kinase complex | 1 |
| intracellular membrane-bounded organelle | 1 |
| intracellular anatomical structure | 1 |
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
1921 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| CCNP | SVOP | Q8N4V2 | 478 |
| CCNP | NAT9 | Q9BTE0 | 457 |
| CCNP | ZNF205 | O95201 | 439 |
| CCNP | STRADA | Q7RTN6 | 409 |
| CCNP | RAD51AP1 | Q96B01 | 391 |
| CCNP | ZFYVE9 | O95405 | 377 |
| CCNP | TMEM220 | Q6QAJ8 | 377 |
| CCNP | C1orf115 | Q9H7X2 | 369 |
| CCNP | SVOPL | Q8N434 | 358 |
| CCNP | COQ9 | O75208 | 349 |
| CCNP | NEU2 | Q9Y3R4 | 323 |
| CCNP | SEC61G | P38384 | 323 |
| CCNP | CDK1 | P06493 | 320 |
| CCNP | PYCR1 | P32322 | 300 |
| CCNP | PLA2G1B | P04054 | 289 |
| CCNP | STK17A | Q9UEE5 | 289 |
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A6QP75, E1BDF2, E2RD63, P0C242, P22674, P29590, P30282, P41155, P48961, P49593, Q13505, Q14094, Q1LZ97, Q32NJ2, Q32NM1, Q3MHH5, Q3TAA7, Q4FZD7, Q52WX2, Q5F2F2, Q5SRT8, Q60I26, Q60I27, Q69Z89, Q6IN84, Q6UXT9, Q70EL4, Q86UR1, Q8BQX5, Q8BTM9, Q8BUM9, Q8N1F8, Q8N2A8, Q8N9H8, Q8TCX5, Q8TDF6, Q8WXI3, Q91ZT7, Q969S2, Q96DC7
Diamond homologs: A0MEB5, A5PK16, O48790, P18606, P20248, P25010, P25011, P30274, P34638, P34800, P34801, P37881, P39963, P41002, P43062, P47827, P51943, P51944, P51986, P78396, Q01J96, Q0DJR9, Q0INT0, Q0JPA4, Q38819, Q39069, Q39071, Q3ECW2, Q5A1N6, Q5XGG5, Q61456, Q6AY13, Q6NYX6, Q7F830, Q7T0L6, Q7TMA5, Q7XSJ6, Q8K4F8, Q92161, Q9C6A9
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
58 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 48 |
| Likely benign | 6 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
1256 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| 19:40223382:GCTCA:G | donor_loss | 1.0000 |
| 19:40223383:CTCA:C | donor_loss | 1.0000 |
| 19:40223384:TCA:T | donor_loss | 1.0000 |
| 19:40223385:CA:C | donor_loss | 1.0000 |
| 19:40223386:A:AT | donor_loss | 1.0000 |
| 19:40223506:C:CT | acceptor_gain | 1.0000 |
| 19:40223506:C:T | acceptor_gain | 1.0000 |
| 19:40223543:CGGG:C | acceptor_gain | 1.0000 |
| 19:40223547:C:CC | acceptor_gain | 1.0000 |
| 19:40224502:A:AC | donor_gain | 1.0000 |
| 19:40224503:C:CC | donor_gain | 1.0000 |
| 19:40224503:CT:C | donor_gain | 1.0000 |
| 19:40224507:T:TA | donor_gain | 1.0000 |
| 19:40224641:CTC:C | acceptor_gain | 1.0000 |
| 19:40223133:T:TA | donor_gain | 0.9900 |
| 19:40223300:TCAC:T | acceptor_gain | 0.9900 |
| 19:40223300:TCACC:T | acceptor_loss | 0.9900 |
| 19:40223301:CACC:C | acceptor_gain | 0.9900 |
| 19:40223301:CACCT:C | acceptor_loss | 0.9900 |
| 19:40223302:ACCTG:A | acceptor_loss | 0.9900 |
| 19:40223303:CCTG:C | acceptor_loss | 0.9900 |
| 19:40223304:C:CC | acceptor_gain | 0.9900 |
| 19:40223305:T:A | acceptor_loss | 0.9900 |
| 19:40223386:A:AC | donor_gain | 0.9900 |
| 19:40223387:C:CC | donor_gain | 0.9900 |
| 19:40223400:C:CA | donor_gain | 0.9900 |
| 19:40223542:GCGGG:G | acceptor_gain | 0.9900 |
| 19:40223543:CGGGC:C | acceptor_gain | 0.9900 |
| 19:40223544:GGG:G | acceptor_gain | 0.9900 |
| 19:40223545:GG:G | acceptor_gain | 0.9900 |
AlphaMissense
1926 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| 19:40224512:T:A | K163N | 0.995 |
| 19:40224512:T:G | K163N | 0.995 |
| 19:40224513:T:A | K163I | 0.994 |
| 19:40223457:G:C | F201L | 0.987 |
| 19:40223457:G:T | F201L | 0.987 |
| 19:40223459:A:G | F201L | 0.987 |
| 19:40224530:G:C | C157W | 0.987 |
| 19:40224531:C:T | C157Y | 0.983 |
| 19:40224532:A:G | C157R | 0.982 |
| 19:40223484:C:A | E192D | 0.980 |
| 19:40223484:C:G | E192D | 0.980 |
| 19:40224519:G:T | A161E | 0.978 |
| 19:40224597:A:G | L135P | 0.978 |
| 19:40224757:G:T | R108S | 0.976 |
| 19:40223485:T:A | E192V | 0.975 |
| 19:40223459:A:T | F201I | 0.963 |
| 19:40223489:C:G | A191P | 0.963 |
| 19:40223511:G:C | F183L | 0.963 |
| 19:40223511:G:T | F183L | 0.963 |
| 19:40223513:A:G | F183L | 0.963 |
| 19:40224618:G:T | T128K | 0.963 |
| 19:40226391:A:G | I84T | 0.961 |
| 19:40224514:T:C | K163E | 0.955 |
| 19:40223458:A:G | F201S | 0.953 |
| 19:40224540:C:T | G154D | 0.953 |
| 19:40223476:A:G | I195T | 0.952 |
| 19:40224603:A:T | V133D | 0.952 |
| 19:40226404:A:G | Y80H | 0.951 |
| 19:40224541:C:G | G154R | 0.950 |
| 19:40223215:G:T | A254D | 0.948 |
dbSNP variants (sampled 300 via entrez): RS1000264091 (19:40223256 G>A,C), RS1000668647 (19:40224901 G>A), RS1001276678 (19:40224710 C>T), RS1002570477 (19:40227209 C>T), RS1003317256 (19:40227112 G>A), RS1003357973 (19:40222303 G>A,C), RS1003631564 (19:40227326 G>A,T), RS1004492683 (19:40222520 T>A,C), RS1004629956 (19:40222335 A>G), RS1004730129 (19:40227150 G>A), RS1004795959 (19:40225595 T>C), RS1004976916 (19:40225009 A>C), RS1005207339 (19:40227336 G>A,C,T), RS1005482488 (19:40227769 T>C), RS1005495679 (19:40223621 C>T)
Disease associations
OMIM: gene MIM:620396 | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
CTD chemical–gene interactions
14 total (human), top 14 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| aristolochic acid I | increases expression | 1 |
| sodium arsenite | decreases expression | 1 |
| CGP 52608 | affects binding, increases reaction | 1 |
| licochalcone B | increases expression | 1 |
| jinfukang | decreases expression | 1 |
| Resveratrol | affects cotreatment, decreases expression | 1 |
| Benzo(a)pyrene | affects methylation, decreases methylation | 1 |
| Plant Extracts | affects cotreatment, decreases expression | 1 |
| Potassium Chloride | decreases response to substance, increases expression | 1 |
| Smoke | decreases expression | 1 |
| Dronabinol | decreases response to substance, increases expression | 1 |
| Tobacco Smoke Pollution | decreases expression | 1 |
| Okadaic Acid | increases expression | 1 |
| Acrylamide | increases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.