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  3. CCNO
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Rare multisystem ciliopathy disorders

Gene: CCNO

Red List (low evidence)
CCNO (cyclin O)
EnsemblGeneIds (GRCh38): ENSG00000152669
EnsemblGeneIds (GRCh37): ENSG00000152669
OMIM: 607752, Gene2Phenotype
CCNO is in 7 panels

1 review

Alice Gardham (Genomics England)

Comment when marking as ready: primary ciliary dyskinesia not included on this panel
Created: 23 Jan 2017, 3:50 p.m.
Created: 23 Jan 2017, 3:50 p.m.

Panel version: 0.429

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Expert list
Phenotypes
  • Ciliary dyskinesia, primary, 29, 615872
OMIM
607752
Clinvar variants
Variants in CCNO
Penetrance
Complete
Panels with this gene

History Filter Activity

26 Jan 2017, Gel status: 1

panel promoted to version 1

Alice Gardham (Genomics England)

Promoted to version 1 by Alice Gardham on 26th January 2017

23 Jan 2017, Gel status: 1

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Red List (Low Evidence).

25 Nov 2016, Gel status: 1

Upload gene information

Ellen McDonagh (Genomics England Curator)

CCNO was added to Rare multisystem ciliopathy disorderspanel. Sources: Radboud University Medical Center, Nijmegen

25 Nov 2016, Gel status: 0

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Phenotypes for gene CCNO were set to Ciliary dyskinesia, primary, 29, 615872

5 Apr 2016, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

CCNO was added to Rare multisystem ciliopathy disorderspanel. Sources: Expert list

5 Apr 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

CCNO was created by ellenmcdonagh