NCF1C pseudogene, associated with a type of white blood cell. It is related to NCF1. It may disable NCF1 by recombination, leading to chronic granulomatous disease.[1]
GULO pseudogene, associated with the production of Vitamin C
Urate oxidase pseudogene, associated with the processing of uric acid
Photolyase pseudogene, associated with repairing DNA damaged by UV radiation.
Photolyase is no longer encoded for despite obvious advantages.[5] Instead, this gene is mutated to encode for cryptochromes.
TLR12P pseudogene, encodes a toll-like receptor.[6] In mice, this gene recognizes profilin.[7] It has also been duplicated in mice into TLR11 (recognizes profilin, bacterial flagellin).[8] TLR13 (recognizes bacterial ribosomal RNA) is another lost TLR, albeit with no appearant pseudogene.[9]
Dubious pseudogenes:
WNT3A. It does encode a functional protein in humans, but has no appearant consequence upon mutation. In mice, loss of the gene causes tail shortening loss.[10]