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)
Paralog prediction (from Ensembl)
Protein motifs (from Interpro)
Gene Ontology (GO)
Pathways (from Reactome) No match
Phenotype (from MGI, Zfin or HPO)
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) No match
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