MYH Polyclonal Antibody, 50ul sgRNA Oligos Mutations in this gene have

Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP)

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or cellular calcium/phosphate homeostasis

GO annotations related to this gene include receptor activity and scavenger receptor activity

The encoded protein could be a spermatogenesis-specific component of the DNA-binding general transcription factor complex TFIID

MYH Polyclonal Antibody, 50ul sgRNA Oligos Mutations in this gene haveMUTYH encodes a DNA glycosylase involved in oxidative DNA damage repair. The enzyme excises adenine bases from the DNA backbone at sites where adenine is inappropriately paired with guanine, cytosine, or 8 oxo 7,8 dihydroguanine, a major oxidatively damaged DNA lesion. A G specific adenine DNA glycosylase is localized to the nucleus and mitochondria. Mutations in this gene result in heritable predisposition to colon and stomach cancer. Multiple