Disease:Defects in EGFL10 are the cause of retinitis pigmentosa type 25 (RP25) [MIM:602772]. RP leads to degeneration of retinal photoreceptor cells. Patients suffer of night blindness, beginning at approximately 25 years of age, and deterioration of visual acuity (central vision), beginning at approximately 30 years of age. By age 55 to 60 years, many affected subjects had no perception of light in either eye.,Function:Required to maintain the integrity of photoreceptor cells.,miscellaneous:Although the protein is conserved in Drosophila, the gene encoding the orthologous protein is inactive in rodents.,similarity:Belongs to the EYS family.,similarity:Contains 27 EGF-like domains.,similarity:Contains 5 laminin G-like domains.,subcellular location:Localizes in the photoreceptor cells layer.,tissue specificity:Present in retina.,
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