ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Naturally occurring read-through transcription occurs

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

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

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

and in a rare syndrome known as alternating hemiplegia of childhood

All family members contain the conserved acyl-Coenzyme A binding domain| which binds acyl-CoA thiol esters

ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Naturally occurring read-through transcription occursThis 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.