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Retinal disorders

Gene: SAMD11

Amber List (moderate evidence)

SAMD11 (sterile alpha motif domain containing 11)
EnsemblGeneIds (GRCh38): ENSG00000187634
EnsemblGeneIds (GRCh37): ENSG00000187634
OMIM: 616765, Gene2Phenotype
SAMD11 is in 2 panels

1 review

Ivone Leong (Genomics England Curator)

I don't know

Submitted on behalf of the GMS Eye specialist group. These genes are also from RetNet. There is currently not enough evidence to rate these genes Green, therefore they have been given an Amber rating.
Created: 27 Dec 2019, 9:10 a.m. | Last Modified: 27 Dec 2019, 9:10 a.m.
Panel Version: 2.5


  • RetNet
  • Expert Review Amber
Clinvar variants
Variants in SAMD11
Panels with this gene

History Filter Activity

27 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

gene: SAMD11 was added gene: SAMD11 was added to Retinal disorders. Sources: Expert Review Amber,RetNet,NHS GMS Mode of inheritance for gene: SAMD11 was set to