C22orf23

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Description

The C22ORF23 (chromosome 22 open reading frame 23) is a protein-coding gene located on chromosome 22.

C22ORF23 is also known as EVG1, dJ1039K5.6.

Associated Diseases

• retinitis pigmentosa
• X-linked retinal dysplasia
• severe early-childhood-onset retinal dystrophy
• reticular dystrophy of the retinal pigment epithelium
• choroidal dystrophy, central areolar, 1
• age related macular degeneration 11
• age related macular degeneration 4
• age related macular degeneration 7
• coloboma of macula
• X-linked retinoschisis
• coloboma of optic nerve
• Stargardt disease 4