Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Glaucoma (developmental)

Gene: FAM161A

Red List (low evidence)

FAM161A (family with sequence similarity 161 member A)
EnsemblGeneIds (GRCh38): ENSG00000170264
EnsemblGeneIds (GRCh37): ENSG00000170264
OMIM: 613596, Gene2Phenotype
FAM161A is in 7 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
Retinitis pigmentosa 28; 606068

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
Retinitis pigmentosa 28, 606068

Details

History Filter Activity

27 Apr 2017, Gel status: 1

panel promoted to version 1

Ellen McDonagh (Genomics England Curator)

27/04/2017: Revised after review and further curation, with clinical input, and promoted to version 1.

11 May 2015, Gel status: 1

Added New Source

Eik Haraldsdottir (Genomics England)

FAM161A was added to Glaucoma (developmental)panel. Sources: Emory Genetics Laboratory