EphA10 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene are

Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN)

RAB6C (RAB6C

The N-terminus of this protein contains elements for localization to cell-extracellular matrix junctions

This gene is present in a gene cluster with other members of the ADAM family on chromosome 8

chromosomal breaks and rearrangements

EphA10 Polyclonal Antibody, 50ul Mechanical Pipette Defects in this gene areEphrin receptors, the largest subfamily of receptor tyrosine kinases (RTKs), and their ephrin ligands are important mediators of cell cell communication regulating cell attachment, shape, and mobility in neuronal and epithelial cells (Aasheim et al. 2005 [PubMed 15777695]). See MIM 179610 for additional background on Eph receptors and ephrins.