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Summary Expression Phenotypes Gene Literature (0) GO Terms (19) Nucleotides (39) Proteins (27) Interactants (3) Wiki
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 :
The rp1l1 gene encodes a photoreceptor-specific protein with wd40 repeats, functioning as a structural component within the connecting cilium and basal body of retinal rod and cone photoreceptors. This...[+]


InterPro :
Doublecortin dom, Doublecortin dom sf, RP1/RP1L1

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Diseases: 


Disease Ontology:
occult macular dystrophy

MIM:
OCCULT MACULAR DYSTROPHY; OCMD

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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