S38A8 Rabbit Polyclonal Antibody, 50ul Pathway and Network Analysis MIM 176730) (Olbrot et al

MIM 176730) (Olbrot et al

MRPL17 (mitochondrial ribosomal protein L17) encodes a 39S subunit protein

where the removal of the extension generates the same form as in the cytoplasm

play a key role in the regulation of eukaryotic gene expression

also referred to as Nettleship-Falls type ocular albinism

S38A8 Rabbit Polyclonal Antibody, 50ul Pathway and Network Analysis MIM 176730) (Olbrot et alThis gene encodes a putative sodium dependent amino acid proton antiporter. The protein has eleven transmembrane domains an extracellular N terminus and an intracellular C terminal tail. The protein is a member of the SLC38 sodium coupled neutral amino acid transporter family of proteins. Mutations in this gene result in foveal hypoplasia with or without optic nerve misrouting and or anterior segment dysgenesis.