EVX2 Rabbit Polyclonal Antibody, 100ul Protein Research Abnormal recombination between PRKX and

Abnormal recombination between PRKX and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females

Multiple transcript variants encoding different isoforms have been found for OPRM1

Inhibited by dual specificity phosphatases

It is a single span type I transmembrane protein that contains a 484 aa extracellular region (aa 31‑514) plus a 68 aa C‑terminal cytoplasmic domain

EVX2 Rabbit Polyclonal Antibody, 100ul Protein Research Abnormal recombination between PRKX andThis gene is located at the 5' end of the HOXD gene cluster on chromosome 2. The encoded protein is a homeobox transcription factor that is related to the protein encoded by the Drosophila even skipped (eve) gene a member of the pair rule class of segmentation genes. A 117 kb microdeletion at the 5' end of the HOXD gene cluster which includes this gene and the HOXD9 HOXD13 genes causes synpolydactyly a dominantly inherited disease resulting in limb