CCNP

gene
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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

FieldValue
HGNC IDHGNC:25805
Approved symbolCCNP
Namecyclin P
Location19q13.2
Locus typegene with protein product
StatusApproved
AliasesFLJ13265
Ensembl geneENSG00000105219
Ensembl biotypeprotein_coding
OMIM620396
Entrez79935

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

ExonStartEnd
ENSE000007064804022448840224643
ENSE000016414764022637540226689
ENSE000016440284022472240224811
ENSE000017884724022338840223546
ENSE000020282294022220840223303

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 IDTPM avgSamples expressed
1809510.183075
1809500.03478
1809490.01263

Top tissues by expression

281 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047398.38gold quality
oocyteCL:000002389.51gold quality
pancreatic ductal cellCL:000207986.25silver quality
right hemisphere of cerebellumUBERON:001489085.85gold quality
cerebellar hemisphereUBERON:000224585.81gold quality
cerebellar cortexUBERON:000212985.57gold quality
cerebellumUBERON:000203783.56gold quality
type B pancreatic cellCL:000016981.34gold quality
olfactory bulbUBERON:000226481.30gold quality
secondary oocyteCL:000065581.26gold quality
metanephros cortexUBERON:001053380.99gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099179.12gold quality
tibialis anteriorUBERON:000138578.75silver quality
superficial temporal arteryUBERON:000161475.18gold quality
right lobe of liverUBERON:000111474.35gold quality
orbitofrontal cortexUBERON:000416774.16gold quality
ileal mucosaUBERON:000033172.68silver quality
pituitary glandUBERON:000000771.55gold quality
triceps brachiiUBERON:000150971.07gold quality
right uterine tubeUBERON:000130271.03gold quality
vastus lateralisUBERON:000137971.02gold quality
biceps brachiiUBERON:000150771.02gold quality
CA1 field of hippocampusUBERON:000388171.02gold quality
adenohypophysisUBERON:000219670.04gold quality
metanephrosUBERON:000008169.61gold quality
gluteal muscleUBERON:000200069.59gold quality
tongue squamous epitheliumUBERON:000691969.45gold quality
upper arm skinUBERON:000426369.40gold quality
parotid glandUBERON:000183169.08gold quality
myocardiumUBERON:000234967.78gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no1.27

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-453499.9966.581907
HSA-MIR-453199.9969.703181
HSA-MIR-605-3P99.8869.221833
HSA-MIR-4728-5P99.8569.394718
HSA-MIR-6785-5P99.8268.684428
HSA-MIR-149-3P99.7268.223963
HSA-MIR-6883-5P99.6968.053785
HSA-MIR-64699.6867.841645
HSA-MIR-444199.4966.563216
HSA-MIR-391599.4568.491905
HSA-MIR-396099.4166.1196
HSA-MIR-584-3P99.3567.691082
HSA-MIR-532-3P99.3465.761195
HSA-MIR-422A99.1865.83550
HSA-MIR-6809-5P99.1368.451223
HSA-MIR-7160-5P99.1167.172207
HSA-MIR-447899.0765.162320
HSA-MIR-427099.0266.261987
HSA-MIR-6754-5P98.6065.541627
HSA-MIR-446398.5666.051071
HSA-MIR-378A-3P98.4366.10548
HSA-MIR-378B98.4365.36573
HSA-MIR-378C98.4366.10548
HSA-MIR-378D98.4366.10548
HSA-MIR-378E98.4365.99551
HSA-MIR-378F98.4365.66554
HSA-MIR-378H98.4366.16545
HSA-MIR-378I98.4366.10548
HSA-MIR-758-3P98.4268.601122
HSA-MIR-807298.2766.2483

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

OrganismSymbolGene ID
danio_rerioccnpENSDARG00000055250
drosophila_melanogasterCycBFBGN0000405
drosophila_melanogasterCycDFBGN0010315
drosophila_melanogasterCycEFBGN0010382
caenorhabditis_elegansWBGENE00000865
caenorhabditis_elegansWBGENE00000866
caenorhabditis_eleganscyb-2.2WBGENE00000867
caenorhabditis_elegansWBGENE00000870
caenorhabditis_eleganscye-1WBGENE00000871

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-PQ9H8S5 (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 IDNamesCanonical?
Q9H8S5-11yes
Q9H8S5-22

RefSeq proteins (2): NP_001398062, NP_079153* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR006671Cyclin_NDomain
IPR013763Cyclin-like_domDomain
IPR036915Cyclin-like_sfHomologous_superfamily
IPR039361CyclinFamily

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)

ModelpLDDTFraction very-high
AF-Q9H8S5-F170.870.38

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:

CategoryTerms
mitotic cell cycle1
mitotic cell cycle phase transition1
cell cycle G1/S phase transition1
cyclin-dependent protein serine/threonine kinase activity1
cyclin-dependent protein kinase regulator activity1
serine/threonine protein kinase complex1
intracellular membrane-bounded organelle1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

1921 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CCNPSVOPQ8N4V2478
CCNPNAT9Q9BTE0457
CCNPZNF205O95201439
CCNPSTRADAQ7RTN6409
CCNPRAD51AP1Q96B01391
CCNPZFYVE9O95405377
CCNPTMEM220Q6QAJ8377
CCNPC1orf115Q9H7X2369
CCNPSVOPLQ8N434358
CCNPCOQ9O75208349
CCNPNEU2Q9Y3R4323
CCNPSEC61GP38384323
CCNPCDK1P06493320
CCNPPYCR1P32322300
CCNPPLA2G1BP04054289
CCNPSTK17AQ9UEE5289

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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance48
Likely benign6
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1256 predictions. Top by Δscore:

VariantEffectΔscore
19:40223382:GCTCA:Gdonor_loss1.0000
19:40223383:CTCA:Cdonor_loss1.0000
19:40223384:TCA:Tdonor_loss1.0000
19:40223385:CA:Cdonor_loss1.0000
19:40223386:A:ATdonor_loss1.0000
19:40223506:C:CTacceptor_gain1.0000
19:40223506:C:Tacceptor_gain1.0000
19:40223543:CGGG:Cacceptor_gain1.0000
19:40223547:C:CCacceptor_gain1.0000
19:40224502:A:ACdonor_gain1.0000
19:40224503:C:CCdonor_gain1.0000
19:40224503:CT:Cdonor_gain1.0000
19:40224507:T:TAdonor_gain1.0000
19:40224641:CTC:Cacceptor_gain1.0000
19:40223133:T:TAdonor_gain0.9900
19:40223300:TCAC:Tacceptor_gain0.9900
19:40223300:TCACC:Tacceptor_loss0.9900
19:40223301:CACC:Cacceptor_gain0.9900
19:40223301:CACCT:Cacceptor_loss0.9900
19:40223302:ACCTG:Aacceptor_loss0.9900
19:40223303:CCTG:Cacceptor_loss0.9900
19:40223304:C:CCacceptor_gain0.9900
19:40223305:T:Aacceptor_loss0.9900
19:40223386:A:ACdonor_gain0.9900
19:40223387:C:CCdonor_gain0.9900
19:40223400:C:CAdonor_gain0.9900
19:40223542:GCGGG:Gacceptor_gain0.9900
19:40223543:CGGGC:Cacceptor_gain0.9900
19:40223544:GGG:Gacceptor_gain0.9900
19:40223545:GG:Gacceptor_gain0.9900

AlphaMissense

1926 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:40224512:T:AK163N0.995
19:40224512:T:GK163N0.995
19:40224513:T:AK163I0.994
19:40223457:G:CF201L0.987
19:40223457:G:TF201L0.987
19:40223459:A:GF201L0.987
19:40224530:G:CC157W0.987
19:40224531:C:TC157Y0.983
19:40224532:A:GC157R0.982
19:40223484:C:AE192D0.980
19:40223484:C:GE192D0.980
19:40224519:G:TA161E0.978
19:40224597:A:GL135P0.978
19:40224757:G:TR108S0.976
19:40223485:T:AE192V0.975
19:40223459:A:TF201I0.963
19:40223489:C:GA191P0.963
19:40223511:G:CF183L0.963
19:40223511:G:TF183L0.963
19:40223513:A:GF183L0.963
19:40224618:G:TT128K0.963
19:40226391:A:GI84T0.961
19:40224514:T:CK163E0.955
19:40223458:A:GF201S0.953
19:40224540:C:TG154D0.953
19:40223476:A:GI195T0.952
19:40224603:A:TV133D0.952
19:40226404:A:GY80H0.951
19:40224541:C:GG154R0.950
19:40223215:G:TA254D0.948

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.

ChemicalActions (top 5)PubMed papers
aristolochic acid Iincreases expression1
sodium arsenitedecreases expression1
CGP 52608affects binding, increases reaction1
licochalcone Bincreases expression1
jinfukangdecreases expression1
Resveratrolaffects cotreatment, decreases expression1
Benzo(a)pyreneaffects methylation, decreases methylation1
Plant Extractsaffects cotreatment, decreases expression1
Potassium Chloridedecreases response to substance, increases expression1
Smokedecreases expression1
Dronabinoldecreases response to substance, increases expression1
Tobacco Smoke Pollutiondecreases expression1
Okadaic Acidincreases expression1
Acrylamideincreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.