ENSG00000152669


Homo sapiens

Features
Gene ID: ENSG00000152669
  
Biological name :CCNO
  
Synonyms : CCNO / cyclin O / P22674
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 5
Strand: -1
Band: q11.2
Gene start: 55231152
Gene end: 55233680
  
Corresponding Affymetrix probe sets: 210021_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000422485
Ensembl peptide - ENSP00000282572
NCBI entrez gene - 10309     See in Manteia.
OMIM - 607752
RefSeq - NM_021147
RefSeq Peptide - NP_066970
swissprot - P22674
Ensembl - ENSG00000152669
  
Related genetic diseases (OMIM): 615872 - Ciliary dyskinesia, primary, 29, 615872
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 FQ311924.1ENSDARG00000099542Danio rerio
 CCNOENSGALG00000028595Gallus gallus
 CcnoENSMUSG00000042417Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
CCNB3 / Q8WWL7 / cyclin B3ENSG0000014708224
CCNB1 / P14635 / cyclin B1ENSG0000013405723
CCNA2 / P20248 / cyclin A2ENSG0000014538623
CCNB2 / O95067 / cyclin B2ENSG0000015745621
CCNA1 / P78396 / cyclin A1ENSG0000013310121
CCND3 / P30281 / cyclin D3ENSG0000011257617
CCNE2 / O96020 / cyclin E2ENSG0000017530517
CCNE1 / P24864 / cyclin E1ENSG0000010517316
CCND1 / P24385 / cyclin D1ENSG0000011009216
CCND2 / P30279 / cyclin D2ENSG0000011897115


Protein motifs (from Interpro)
Interpro ID Name
 IPR004367  Cyclin, C-terminal domain
 IPR006671  Cyclin, N-terminal
 IPR013763  Cyclin-like
 IPR028864  Cyclin-O
 IPR036915  Cyclin-like superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000278 mitotic cell cycle IDA
 biological_processGO:0006284 base-excision repair IDA
 biological_processGO:0007049 cell cycle IEA
 biological_processGO:0030030 cell projection organization IEA
 biological_processGO:0042493 response to drug IEA
 biological_processGO:0051301 cell division IEA
 biological_processGO:0060271 cilium assembly IMP
 biological_processGO:1903251 multi-ciliated epithelial cell differentiation IMP
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IEA
 molecular_functionGO:0004844 uracil DNA N-glycosylase activity IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000789 Infertility 
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 HP:0002110 Bronchiectasis 
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 HP:0002205 Recurrent respiratory infections 
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 HP:0003676 Progressive disorder 
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 HP:0012265 Ciliary dyskinesia "A deviation from the normally well coordinated pattern of intracellular and intercellular synchrony of motile cilia. Dyskinetic cilia usually beat out of synchrony relative to neighboring cilia." [HPO:probinson, pmid:19606528]
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 HP:0100750 Atelectasis 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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