CCNO (cyclin O)

2003-02-01 Affiliation

Identity

HGNC

CCNO

LOCATION

5q11.2

LOCUSID

10309

ALIAS

CCNU,CILD29,UDG2

FUSION GENES

Show Gene Fusions

Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool

Other Information

Locus ID:

NCBI: 10309
MIM: 607752
HGNC: 18576
Ensembl: ENSG00000152669

Variants:

dbSNP: 10309
ClinVar: 10309
TCGA: ENSG00000152669
COSMIC: CCNO

RNA/Proteins

Gene ID	Transcript ID	Uniprot
ENSG00000152669	ENST00000282572	P22674
ENSG00000152669	ENST00000501463	P22674

Expression (GTEx)

Adipose - Subcutaneous

Adipose - Visceral

Adrenal Gland

Artery - Aorta

Artery - Tibial

Bladder

Brain - Amygdala

Brain - Anterior cingulate cortex

Brain - Caudate

Brain - Cerebellar Hemisphere

Brain - Cerebellum

Brain - Cortex

Brain - Frontal Cortex

Brain - Hippocampus

Brain - Hypothalamus

Brain - Nucleus accumbens

Brain - Putamen

Brain - Spinal cord

Brain - Substantia nigra

Breast - Mammary Tissue

Cells - Cultured fibroblasts

Cells - EBV - transformed lymphocytes

Cervix - Ectocervix

Cervix - Endocervix

Colon - Sigmoid

Colon - Transverse

Esophagus - Gastroesophageal Junction

Esophagus - Mucosa

Esophagus - Muscularis

Fallopian Tube

Heart - Atrial Appendage

Heart - Left Ventricle

Kidney - Cortex

Kidney - Medulla

Liver

Lung

Minor Salivary Gland

Muscle - Skeletal

Nerve - Tibial

Ovary

Pancreas

Pituitary

Prostate

Skin - Not Sun Exposed

Skin - Sun Exposed

Small Intestine - Terminal Ileum

Spleen

Stomach

Testis

Thyroid

Uterus

Vagina

Whole Blood

Protein levels (Protein atlas)

Not detected

Low

Medium

High

References

Pubmed ID	Year	Title	Citations
34102041	2021	Primary ciliary dyskinesia due to CCNO mutations-A genotype-phenotype correlation contribution.	7
34569065	2021	Bi-allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport.	5
34102041	2021	Primary ciliary dyskinesia due to CCNO mutations-A genotype-phenotype correlation contribution.	7
34569065	2021	Bi-allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport.	5
26777464	2016	Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.	41
27571178	2016	The DDB1-DCAF1-Vpr-UNG2 crystal structure reveals how HIV-1 Vpr steers human UNG2 toward destruction.	55
26777464	2016	Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.	41
27571178	2016	The DDB1-DCAF1-Vpr-UNG2 crystal structure reveals how HIV-1 Vpr steers human UNG2 toward destruction.	55
24747639	2014	Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.	118
24747639	2014	Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.	118
8419333	1993	Cell cycle regulation of a human cyclin-like gene encoding uracil-DNA glycosylase.	14
8419333	1993	Cell cycle regulation of a human cyclin-like gene encoding uracil-DNA glycosylase.	14
2001396	1991	Isolation and characterization of a human cDNA encoding uracil-DNA glycosylase.	20
2001396	1991	Isolation and characterization of a human cDNA encoding uracil-DNA glycosylase.	20

Citation

Dessen P

CCNO (cyclin O)

Atlas Genet Cytogenet Oncol Haematol. 2003-02-01

Online version: http://atlasgeneticsoncology.org/gene/42768/haematological-explorer/teaching-explorer/css/template-nav.css