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ARMS2

Involvement in disease

Macular degeneration, age-related, 8

ARMD8

A form of age-related macular degeneration, a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.

None

Disease susceptibility is associated with variants affecting the gene represented in this entry.

Tissue Specificity

Detected in retina and placenta.

Cellular localization

Alternative names

Age-related maculopathy susceptibility protein 2, ARMS2

swissprot:P0C7Q2 omim:611313 entrezGene:387715