EVX2 Rabbit Polyclonal Antibody, 100ul Protein Research Interacts with SMN1 AND GEMIN4

Interacts with SMN1 AND GEMIN4

|miscellaneous:G0-restricted expression

Multiple transcript variants encoding different isoforms have been found for OPRM1

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

Inhibited by dual specificity phosphatases

EVX2 Rabbit Polyclonal Antibody, 100ul Protein Research Interacts with SMN1 AND GEMIN4This 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