Glucose metabolism is highly affected in IRDs associated with variants involved in the glycolysis pathway, such as HK1 [61,62] and HKDC1 [63] associated with autosomal dominant or recessive RP, respectively; and in two retinal degeneration mouse models, rd2 and rd10, characterised by decreased levels of GLUT1 protein [64]. The gene discussed is HKDC1; the disease is retinitis pigmentosa 1.