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  2. Ophthalmological ciliopathies
  3. CCDC28B
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Ophthalmological ciliopathies

Gene: CCDC28B

Red List (low evidence)
CCDC28B (coiled-coil domain containing 28B)
EnsemblGeneIds (GRCh38): ENSG00000160050
EnsemblGeneIds (GRCh37): ENSG00000160050
OMIM: 610162, Gene2Phenotype
CCDC28B is in 12 panels

3 reviews

Beth Hoskins (Great Ormond Street Hospital)

I don't know

Created: 5 Nov 2017, 2:44 a.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version Imported from "Bardet-Biedl Syndrome" panel version 0

Ellen McDonagh (Genomics England Curator)

Comment on list classification: Modifier gene.
Created: 12 Dec 2016, 12:45 p.m.
Comment on list classification: Modifier gene.
Created: 12 Dec 2016, 12:45 p.m.
Created: 12 Dec 2016, 12:45 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version 0.362

Caroline Wright (Genomics England Curator)

Comment when marking as ready: OMIM: likely modifier, one patient only
Created: 17 Dec 2015, 2:14 p.m.
Created: 17 Dec 2015, 2:14 p.m.

Panel version: Imported from Rare multisystem ciliopathy disorders panel version Imported from "Bardet-Biedl Syndrome" panel version 0.5

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • UKGTN
  • Expert Review Red
  • Expert list
  • Emory Genetics Laboratory
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • ciliopathies
  • {Bardet-Biedl syndrome 1, modifier of}, 209900
OMIM
610162
Clinvar variants
Variants in CCDC28B
Penetrance
None
Publications
Panels with this gene

History Filter Activity

8 Jul 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: CCDC28B was added gene: CCDC28B was added to Ophthalmological ciliopathies. Sources: Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Expert list,Expert Review Red,UKGTN Mode of inheritance for gene: CCDC28B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CCDC28B were set to 23015189 Phenotypes for gene: CCDC28B were set to ciliopathies; {Bardet-Biedl syndrome 1, modifier of}, 209900