ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene have

Mutations in this gene have been associated with pontocerebellar hypoplasia type 2

Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix

stability and cross-linking by catalyzing post-translational 3-hydroxylation of proline residues

Naturally occurring read-through transcription occurs between this locus and the neighboring locus HSPE1

ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene haveThis gene encodes a 2 C methyl D erythritol 4 phosphate cytidylyltransferase like protein. Mutations in this gene are the cause of Walker Warburg syndrome. Alternate splicing results in multiple transcript variants.