Structural eye disease
Gene: CDHR1

CDHR1 (cadherin related family member 1)
EnsemblGeneIds (GRCh38): ENSG00000148600
EnsemblGeneIds (GRCh37): ENSG00000148600
OMIM: 609502, Gene2Phenotype
CDHR1 is in 3 panels

2 reviews

Nicola Ragge (Birmingham Women's and Children's NHS Foundation Hospital Trust)

Red List (low evidence)

retinal gene, can't find any evidence that it is associated with structural eye disease
Created: 19 Jun 2019, 3:32 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Cone-rod dystrophy 15; 613660

Created: 19 Jun 2019, 3:32 p.m.

Panel version: 0.76

Ivone Leong (Genomics England Curator)

Red List (low evidence)

Submitted on behalf of Professor Nicola Ragge (Wessex and West Midlands GLH). retinal gene, can't find any evidence that it is associated with structural eye disease
Created: 17 Apr 2019, 3:30 p.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Cone-rod dystrophy 15, 613660

Created: 17 Apr 2019, 3:30 p.m.

Panel version: 0.38

Details

Mode of Inheritance

BIALLELIC, autosomal or pseudoautosomal

Sources

NHS GMS
Expert Review Red

Phenotypes

Cone-rod dystrophy 15, 613660
Eye Disorders

OMIM

609502

Clinvar variants

Variants in CDHR1

Penetrance

None

Panels with this gene

History Filter Activity

17 Apr 2019, Gel status: 1

Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to CDHR1. Mode of inheritance for gene CDHR1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Cone-rod dystrophy 15, 613660 for gene: CDHR1

3 Jan 2019, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: CDHR1 was added gene: CDHR1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CDHR1 was set to Phenotypes for gene: CDHR1 were set to Eye Disorders

Structural eye disease Gene: CDHR1