Structural eye disease
Gene: PRPF31

PRPF31 (pre-mRNA processing factor 31)
EnsemblGeneIds (GRCh38): ENSG00000105618
EnsemblGeneIds (GRCh37): ENSG00000105618
OMIM: 606419, Gene2Phenotype
PRPF31 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
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Retinitis pigmentosa 11; 600138

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
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Phenotypes
Retinitis pigmentosa 11, 600138

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

Panel version: 0.48

Details

Mode of Inheritance

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Sources

NHS GMS
Expert Review Red

Phenotypes

Retinitis pigmentosa 11, 600138
Eye Disorders

OMIM

606419

Clinvar variants

Variants in PRPF31

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 PRPF31. Mode of inheritance for gene PRPF31 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 11, 600138 for gene: PRPF31

3 Jan 2019, Gel status: 1

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

Ellen McDonagh (Genomics England Curator)

gene: PRPF31 was added gene: PRPF31 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: PRPF31 was set to Phenotypes for gene: PRPF31 were set to Eye Disorders

Structural eye disease Gene: PRPF31