CCNJ

gene
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Also known as FLJ10895bA690P14.1

Summary

CCNJ (cyclin J, HGNC:23434) is a protein-coding gene on chromosome 10q24.1, encoding Cyclin-J (Q5T5M9).

Predicted to enable cyclin-dependent protein serine/threonine kinase regulator activity. Predicted to be involved in G1/S transition of mitotic cell cycle. Predicted to be part of cyclin-dependent protein kinase holoenzyme complex. Predicted to be active in cytoplasm; microtubule organizing center; and nucleus.

Source: NCBI Gene 54619 — RefSeq curated summary.

At a glance

  • GWAS associations: 2
  • Clinical variants (ClinVar): 48 total
  • MANE Select transcript: NM_001134375

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:23434
Approved symbolCCNJ
Namecyclin J
Location10q24.1
Locus typegene with protein product
StatusApproved
AliasesFLJ10895, bA690P14.1
Ensembl geneENSG00000107443
Ensembl biotypeprotein_coding
OMIM620395
Entrez54619

Gene structure

Transcript identifiers

Ensembl transcripts: 12 — 12 protein_coding

ENST00000265992, ENST00000403870, ENST00000465148, ENST00000868256, ENST00000918738, ENST00000918739, ENST00000918740, ENST00000918741, ENST00000918742, ENST00000918743, ENST00000918744, ENST00000918745

RefSeq mRNA: 3 — MANE Select: NM_001134375 NM_001134375, NM_001134376, NM_019084

CCDS: CCDS44462, CCDS44463, CCDS7445

Canonical transcript exons

ENST00000465148 — 6 exons

ExonStartEnd
ENSE000008110179605670196057000
ENSE000013446599605025696050466
ENSE000016467949605708896057247
ENSE000018760109604358396043719
ENSE000021942199604435396044462
ENSE000032865979605783096060870

Expression profiles

Bgee: expression breadth ubiquitous, 252 present calls, max score 98.76.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 10.0609 / max 125.6237, expressed in 1769 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1063709.86661768
1063710.180079
1063690.01433

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
secondary oocyteCL:000065598.76gold quality
oocyteCL:000002398.20gold quality
buccal mucosa cellCL:000233689.02gold quality
embryoUBERON:000092283.66gold quality
ganglionic eminenceUBERON:000402383.40gold quality
ventricular zoneUBERON:000305382.21gold quality
monocyteCL:000057681.79gold quality
mononuclear cellCL:000084281.60gold quality
cortical plateUBERON:000534381.36gold quality
leukocyteCL:000073881.16gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047379.94gold quality
medial globus pallidusUBERON:000247777.24silver quality
endometriumUBERON:000129577.03gold quality
globus pallidusUBERON:000187576.06silver quality
islet of LangerhansUBERON:000000675.89gold quality
right adrenal gland cortexUBERON:003582775.41gold quality
stromal cell of endometriumCL:000225575.40gold quality
granulocyteCL:000009474.81gold quality
bone marrowUBERON:000237174.78gold quality
left adrenal glandUBERON:000123474.47gold quality
adrenal cortexUBERON:000123574.37gold quality
left adrenal gland cortexUBERON:003582574.32gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099173.97gold quality
right adrenal glandUBERON:000123373.84gold quality
lymph nodeUBERON:000002973.81gold quality
adrenal glandUBERON:000236973.65gold quality
adrenal tissueUBERON:001830373.39gold quality
rectumUBERON:000105273.33gold quality
gall bladderUBERON:000211073.12gold quality
spleenUBERON:000210673.02gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.21

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

194 targeting CCNJ, 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-200B-3P100.0073.312693
HSA-MIR-200C-3P100.0073.352685
HSA-MIR-429100.0073.442698
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-4262100.0073.263931
HSA-MIR-29A-3P100.0073.111835
HSA-MIR-29B-3P100.0073.181833
HSA-MIR-29C-3P100.0073.151833
HSA-MIR-4682100.0068.891258
HSA-MIR-340-5P100.0072.504437
HSA-MIR-196A-5P100.0068.16684
HSA-MIR-196B-5P100.0068.16681
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-513A-5P100.0069.772465
HSA-MIR-450099.9972.722367
HSA-MIR-371B-5P99.9975.344759
HSA-MIR-181A-5P99.9972.962995
HSA-MIR-181B-5P99.9972.972996
HSA-MIR-181C-5P99.9972.952996
HSA-MIR-181D-5P99.9973.042997
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-373-5P99.9875.364753
HSA-MIR-616-5P99.9875.584775
HSA-LET-7A-5P99.9872.291790
HSA-LET-7B-5P99.9872.311790
HSA-LET-7C-5P99.9872.291790
HSA-LET-7E-5P99.9872.291790
HSA-LET-7F-5P99.9872.561784
HSA-LET-7G-5P99.9872.371784

Literature-anchored findings (GeneRIF, showing 5)

  • miR-125b acts as a tumor suppressor in breast tumorigenesis via its novel direct targets ENPEP, CK2-alpha, CCNJ, and MEGF9. (PMID:24098452)
  • In conclusion, our results indicated that CCNJ could be a novel prognostic marker of HCC, and this study indicated that triple combination array analysis was effective in detecting new tumor-related genes and their mechanisms. (PMID:25672416)
  • CCNJ is a target of miR205 mediated downregulation in bladder cancer cells. (PMID:26469956)
  • we identified cyclin J and far upstream element-binding protein 1 (FUBP1) as novel miR-16 targets, which mediate miR-16 antiproliferative effects. (PMID:27157613)
  • High Cyclin J expression is associated with drug resistance in non-small cell lung cancer. (PMID:28202053)

Cross-species orthologs

15 orthologs

OrganismSymbolGene ID
danio_rerioccnjENSDARG00000059917
mus_musculusCcnjENSMUSG00000025010
rattus_norvegicusCcnjENSRNOG00000076838
drosophila_melanogasterCycAFBGN0000404
drosophila_melanogasterCycBFBGN0000405
drosophila_melanogasterCycDFBGN0010315
drosophila_melanogasterCycEFBGN0010382
caenorhabditis_elegansWBGENE00000863
caenorhabditis_elegansWBGENE00000864
caenorhabditis_elegansWBGENE00000865
caenorhabditis_elegansWBGENE00000866
caenorhabditis_eleganscyb-2.2WBGENE00000867
caenorhabditis_elegansWBGENE00000870
caenorhabditis_eleganscye-1WBGENE00000871
caenorhabditis_elegansWBGENE00017259

Paralogs (18): CCNE1 (ENSG00000105173), CCNP (ENSG00000105219), 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-JQ5T5M9 (reviewed: Q5T5M9)

All UniProt accessions (1): Q5T5M9

UniProt curated annotations — full annotation on UniProt →

Similarity. Belongs to the cyclin family.

Isoforms (3)

UniProt IDNamesCanonical?
Q5T5M9-11yes
Q5T5M9-22
Q5T5M9-33

RefSeq proteins (3): NP_001127847, NP_001127848, NP_061957 (=MANE)

Domains & families (InterPro)

IDNameType
IPR004367Cyclin_C-domDomain
IPR006671Cyclin_NDomain
IPR013763Cyclin-like_domDomain
IPR036915Cyclin-like_sfHomologous_superfamily
IPR039361CyclinFamily

Pfam: PF00134, PF02984

UniProt features (4 total): splice variant 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5T5M9-F173.340.59

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 220 (showing top): ACTACCT_MIR196A_MIR196B, TGCACTT_MIR519C_MIR519B_MIR519A, GOBP_CELL_CYCLE_PHASE_TRANSITION, AAAYRNCTG_UNKNOWN, CAGCTG_AP4_Q5, GOCC_MICROTUBULE_ORGANIZING_CENTER, CAGCAGG_MIR370, SOX9_B1, MCAATNNNNNGCG_UNKNOWN, GOBP_CELL_CYCLE_G1_S_PHASE_TRANSITION, GOBP_MITOTIC_CELL_CYCLE, RASHI_RESPONSE_TO_IONIZING_RADIATION_6, SOX5_01, GOCC_TRANSFERASE_COMPLEX_TRANSFERRING_PHOSPHORUS_CONTAINING_GROUPS, GOCC_TRANSFERASE_COMPLEX

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 (4): cyclin-dependent protein kinase holoenzyme complex (GO:0000307), nucleus (GO:0005634), cytoplasm (GO:0005737), microtubule organizing center (GO:0005815)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure2
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
microtubule cytoskeleton1

Protein interactions and networks

STRING

864 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CCNJMEGF9Q9H1U4571
CCNJFUBP1Q96AE4418
CCNJCSNK2A2P19784384
CCNJZNF408Q9H9D4374
CCNJGRAMD4Q6IC98374
CCNJENPEPQ07075371
CCNJCC2D2BQ6DHV5351
CCNJCCNCP24863340
CCNJACOT13Q9NPJ3321
CCNJCCNHP51946317
CCNJAKAP7O43687309
CCNJBTBD9Q96Q07306
CCNJGP9P14770301
CCNJNMUR1Q9HB89301
CCNJNHSL3Q9P206294

IntAct

11 interactions, top by confidence:

ABTypeScore
CDK2CCNE2psi-mi:“MI:0914”(association)0.940
CDK2GMNNpsi-mi:“MI:0914”(association)0.640
GORASP1PPP6R2psi-mi:“MI:0914”(association)0.530
CCNJPOTEFpsi-mi:“MI:0915”(physical association)0.400
GORASP1RTCApsi-mi:“MI:0914”(association)0.350
BCL11BMTA2psi-mi:“MI:0914”(association)0.350
NOBOXCDK2psi-mi:“MI:0914”(association)0.350
GORASP1PRORPpsi-mi:“MI:0914”(association)0.350
CCNJATE1psi-mi:“MI:0914”(association)0.350
SLC30A5NBASpsi-mi:“MI:0914”(association)0.350

BioGRID (12): CCNJ (Affinity Capture-MS), POTEF (Affinity Capture-MS), SPECC1L (Affinity Capture-MS), CCNJ (Affinity Capture-MS), CCNJ (Affinity Capture-MS), POTEF (Affinity Capture-MS), CCNJ (Affinity Capture-MS), CCNJ (Affinity Capture-MS), CCNJ (Affinity Capture-MS), CCNJ (Affinity Capture-RNA), CCNJ (Affinity Capture-RNA), CCNJ (Affinity Capture-MS)

ESM2 similar proteins: A5PK16, O08918, O42575, O96020, P24385, P24864, P25322, P30279, P30280, P30282, P39948, P39949, P39950, P41002, P47794, P48961, P49706, P49707, P50755, P50756, P51944, P51945, P51959, P53782, P55169, Q04827, Q0P5D3, Q16589, Q2KI22, Q32NJ2, Q32NM1, Q52QT8, Q5E9I1, Q5E9K7, Q5R5D0, Q5R6J5, Q5SRT8, Q5T5M9, Q5XGG5, Q61457

Diamond homologs: C4YR54, O48790, P0CY18, P13351, P13365, P20437, P20438, P24861, P24865, P24868, P24869, P24870, P24871, P25009, P25011, P25012, P30284, P32943, P34800, P34801, P37881, P39963, P43062, P51986, Q06374, Q0DH40, Q0JIF2, Q10Q62, Q10QA2, Q39068, Q39069, Q39070, Q3TZI6, Q59YH3, Q5A0A9, Q5A1N6, Q5T5M9, Q659K0, Q6DFJ9, Q810T2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

48 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance37
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

918 predictions. Top by Δscore:

VariantEffectΔscore
10:96044458:ACAAG:Adonor_loss1.0000
10:96044459:CAAG:Cdonor_loss1.0000
10:96044460:AAGGT:Adonor_loss1.0000
10:96044461:AGGT:Adonor_loss1.0000
10:96044462:GGTAA:Gdonor_loss1.0000
10:96044463:GT:Gdonor_loss1.0000
10:96044464:T:Adonor_loss1.0000
10:96050463:GCAA:Gdonor_gain1.0000
10:96050464:CAAG:Cdonor_loss1.0000
10:96050465:AAGT:Adonor_loss1.0000
10:96050466:AGTA:Adonor_loss1.0000
10:96050467:G:GGdonor_gain1.0000
10:96050467:G:Tdonor_loss1.0000
10:96050468:T:Adonor_loss1.0000
10:96056985:G:GTdonor_gain1.0000
10:96056997:CAAG:Cdonor_loss1.0000
10:96057001:GTGG:Gdonor_loss1.0000
10:96057245:GAT:Gdonor_gain1.0000
10:96057248:G:GGdonor_gain1.0000
10:96057821:A:AGacceptor_gain1.0000
10:96057821:AC:Aacceptor_gain1.0000
10:96057822:C:CAacceptor_gain1.0000
10:96057822:C:Gacceptor_gain1.0000
10:96057825:TTCAG:Tacceptor_loss1.0000
10:96057826:TCA:Tacceptor_loss1.0000
10:96057827:CAGC:Cacceptor_loss1.0000
10:96057828:A:AGacceptor_gain1.0000
10:96057828:AG:Aacceptor_loss1.0000
10:96057828:AGC:Aacceptor_gain1.0000
10:96057829:G:GAacceptor_gain1.0000

AlphaMissense

2488 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
10:96044452:T:CL20P1.000
10:96050305:G:CR40T1.000
10:96050305:G:TR40I1.000
10:96050306:A:CR40S1.000
10:96050306:A:TR40S1.000
10:96050328:G:CA48P1.000
10:96050374:T:CL63P1.000
10:96050376:G:CA64P1.000
10:96050389:T:CL68P1.000
10:96050392:A:CD69A1.000
10:96050392:A:TD69V1.000
10:96050431:T:CL82P1.000
10:96050451:T:CC89R1.000
10:96050452:G:AC89Y1.000
10:96050453:C:GC89W1.000
10:96050455:T:CL90P1.000
10:96056705:A:CK95N1.000
10:96056705:A:TK95N1.000
10:96056730:C:TP104S1.000
10:96056731:C:AP104H1.000
10:96056746:T:CL109P1.000
10:96056838:T:AW140R1.000
10:96056838:T:CW140R1.000
10:96056840:G:CW140C1.000
10:96056840:G:TW140C1.000
10:96056854:C:AP145Q1.000
10:96057145:C:GS202W1.000
10:96057148:G:CR203T1.000
10:96057148:G:TR203M1.000
10:96057149:G:CR203S1.000

dbSNP variants (sampled 300 via entrez): RS1000079410 (10:96042949 G>A,C), RS1000187916 (10:96051560 T>C), RS1000237337 (10:96060271 C>T), RS1000296120 (10:96042755 C>G,T), RS1000391610 (10:96042390 A>G), RS1000510206 (10:96047422 T>C), RS1000540863 (10:96047186 A>G), RS1000552190 (10:96055664 T>A), RS1000611042 (10:96055356 C>A,T), RS1000772419 (10:96060572 G>A), RS1000809700 (10:96054035 C>G), RS1001055142 (10:96041601 A>G), RS1001073455 (10:96054442 G>A,C), RS1001185405 (10:96044889 A>C,T), RS1001453952 (10:96047869 A>G)

Disease associations

OMIM: gene MIM:620395 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

2 associations (top):

StudyTraitp-value
GCST005863_28Menopause (age at onset)3.000000e-22
GCST005863_32Menopause (age at onset)2.000000e-20

EFO canonical traits (1, from GWAS)

EFO IDTrait name
EFO:0004704age at menopause

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

38 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, decreases expression3
Benzo(a)pyrenedecreases expression, decreases methylation2
Particulate Matterdecreases reaction, increases expression, increases abundance2
trichostatin Aaffects expression1
tris(1,3-dichloro-2-propyl)phosphateincreases expression1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
manganese chlorideincreases abundance, increases expression, affects cotreatment1
CGP 52608affects binding, increases reaction1
2-palmitoylglycerolincreases expression1
entinostatdecreases expression1
scriptaidaffects expression1
motexafin gadoliniumaffects cotreatment, decreases expression1
2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amidedecreases reaction, increases expression1
bisphenol Saffects cotreatment, increases expression1
jinfukangdecreases expression1
Leflunomideincreases expression1
Air Pollutantsincreases abundance, increases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Aspirinincreases expression1
Vehicle Emissionsdecreases reaction, increases expression1
Dexamethasoneaffects cotreatment, increases expression1
Estradiolincreases expression1
Formaldehydedecreases expression1
Hydrogen Peroxideaffects expression1
Indomethacinincreases expression, affects cotreatment1
Leadaffects expression1
Manganeseincreases abundance, increases expression, affects cotreatment1
Melphalanincreases expression1
Methyl Methanesulfonatedecreases expression1
Smokedecreases expression1

Cellosaurus cell lines

1 cell lines: 1 cancer cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_SH44HAP1 CCNJ (-)Cancer cell lineMale

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.