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Retinal disorders

Gene: AMN

Red List (low evidence)

AMN (amnion associated transmembrane protein)
EnsemblGeneIds (GRCh38): ENSG00000166126
EnsemblGeneIds (GRCh37): ENSG00000166126
OMIM: 605799, Gene2Phenotype
AMN is in 11 panels

2 reviews

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

Red List (low evidence)

remove
Created: 30 Aug 2019, 2:12 p.m. | Last Modified: 30 Aug 2019, 2:12 p.m.
Panel Version: 1.159

Ellen McDonagh (Genomics England Curator)

Red List (low evidence)

No relevant association found in OMIM or Gene2Phenotype.
Created: 1 Jun 2016, 10:54 a.m.

History Filter Activity

3 Apr 2019, Gel status: 1

Added New Source

Ivone Leong (Genomics England Curator)

Source NHS GMS was added to AMN.

9 Mar 2016, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

AMN was created by ellenmcdonagh

9 Mar 2016, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

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