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Symbol RP2 contributors: npt/mct/shn/pgu - updated : 25-08-2017
HGNC name retinitis pigmentosa 2 (X-linked recessive)
HGNC id 10274
ASSOCIATED DISORDERS
corresponding disease(s) RP2
related resource Retinal Information Network
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
Xp11.3 microdeletion with association of RP and mental retardation
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS