GeneSet Information

Tier I GS171631 • HP:0008051 Abnormality of the retinal pigment epithelium

DESCRIPTION:

"An abnormality of the `retinal pigment epithelium` (FMA:58627). Much of the pigmentary change that occurs in diseases of the retina takes place in the RPE (which is pigmented) rather than in the retina (which is transparent). The main purpose of the RPE is to insulate and support the overlying neural retina." [HPO:probinson]

LABEL:

HP:0008051

SCORE TYPE:

Binary

DATE ADDED:

2012-11-08

DATE UPDATED:

2024-04-25

SPECIES:

No publication information is associated with this GeneSet.

Annotation Information

No sequence read archive data associated with this GeneSet.

Gene List • 201 Genes

Uploaded As Gene Symbol Homology Score Priority LinkOuts Emphasis