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GENE - TERM ANNOTATION REPORT

RGD ID: 732783
Species: Homo sapiens
RGD Object: Gene
Symbol: KL
Name: klotho
Acc ID: DOID:10584
Term: retinitis pigmentosa
Definition: A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Retinitis_pigmentosa "DO" "DO", http://ghr.nlm.nih.gov/condition/retinitis-pigmentosa "DO" "DO", http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043609/ "DO" "DO", https://www.genome.gov/Genetic-Disorders/Retinitis-Pigmentosa "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
KL ISOKl (Rattus norvegicus)10403060RGDprotein:increased expression:retina,photoreceptor,nucleus: 
KL ISOKl (Mus musculus)10403060RGDprotein:increased expression:retina,photoreceptor,nucleus: 
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