XB-GENEPAGE-960508
???displayGene.symbol???:
rp1l1
???displayGene.name???:
retinitis pigmentosa 1 like 1
???displayGene.synonyms???
LOC108717243
(
Nomenclature history )
???displayGene.geneFunction???
Microtubule assembly protein Doublecortin and related proteins, contain DCX domain
AI Protein Function
:
rp1l1 encodes a microtubule‑associated protein that functions in photoreceptor outer segment morphogenesis. The protein is localized to the connecting cilium and outer segment axoneme of photoreceptor ...[+]
???displayGene.geneInteractants???
Loading ...
Diseases:
Disease Ontology:
occult macular dystrophy
MIM:
OCCULT MACULAR DYSTROPHY; OCMD
External Links:
Loading gene data...
Please wait while we fetch the latest information
| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
|
|
|
|||||||||||
| More Information |
|
|||||||||||
Symbol legend:
