SH3G1 Rabbit Polyclonal Antibody, 20ul Custom Peptide Synthesis Defects in this gene are

Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59)

Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets

Read-through transcripts that include exons from the downstream gene LOC389458 are expressed from this locus

PAK4 is a mediator of filopodia formation and may play a role in the reorganization of the actin cytoskeleton

have been found for PEX11B

SH3G1 Rabbit Polyclonal Antibody, 20ul Custom Peptide Synthesis Defects in this gene areThis gene encodes a member of the endophilin family of Src homology 3 domain containing proteins. The encoded protein is involved in endocytosis and may also play a role in the cell cycle. Overexpression of this gene may play a role in leukemogenesis and the encoded protein has been implicated in acute myeloid leukemia as a fusion partner of the myeloid lymphoid leukemia protein. Pseudogenes of this gene are located on the long arm of chromosomes 11