Retinitis Pigmentosa 30 (RP30)

Alias:
Rp30
Retinitis Pigmentosa, Type 30
Retinitis Pigmentosa-30
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Retinitis Pigmentosa 30, also known as rp30, is related to fundus dystrophy and retinitis pigmentosa. An important gene associated with Retinitis Pigmentosa 30 is FSCN2 (Fascin Actin-Bundling Protein 2, Retinal), and among its related pathways/superpathways are Neurophysiological process Glutamate regulation of Dopamine D1A receptor signaling and Unblocking of NMDA receptors, glutamate binding and activation. Affiliated tissues include retina and eye, and related phenotypes are visual impairment and optic atrophy
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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