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Retinal disorders

Gene: CUBN

Red List (low evidence)

CUBN (cubilin)
EnsemblGeneIds (GRCh38): ENSG00000107611
EnsemblGeneIds (GRCh37): ENSG00000107611
OMIM: 602997, Gene2Phenotype
CUBN is in 8 panels

1 review

Gavin Arno (UCL Institute of Ophthalmology/Moorfields Eye Hospital)

Red List (low evidence)

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Megaloblastic anemia-1, Finnish type
OMIM
602997
Clinvar variants
Variants in CUBN
Penetrance
Complete
Panels with this gene

History Filter Activity

3 Apr 2019, Gel status: 1

Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to CUBN.

9 Mar 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

CUBN was created by ellenmcdonagh

9 Mar 2016, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

CUBN was added to Posterior segment abnormalitiespanel. Sources: Expert Review Red