| Entrez gene ID | | 271209 |
| Official gene symbol | | Rp1l1 |
| Full name | | retinitis pigmentosa 1 homolog (human)-like 1 |
| Aliases | | BC031365,BE983540,Dcdc4,MGC38744,Rp1hl1 |
| Gene summary | | This gene encodes a member of the doublecortin family. This protein is a retinal-specific protein. It contains two N-terminal doublecortin domains, which can assemble and stabilize axonemal microtubules, but lacks the C-terminal repetitive regions including the 16aa repeat found in human RP1L1. This protein and the RP1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. [provided by RefSeq] |
| Location | | Chromosome: 14 Locus: 14 D1 |
| Gene position | | 64611268 - 64652343 Map Viewer |
| Gene orientation | | plus |
| Gene size | | 41076 bp |
| Gene sequence |
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