TSN1 Rabbit Polyclonal Antibody, 20ul Lysosome A related family member

A related family member

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presumably reflecting diverse functions in vivo

Allelic variants of this gene are associated with the autosomal-recessive disorder Joubert syndrome

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

TSN1 Rabbit Polyclonal Antibody, 20ul Lysosome A related family memberThe protein encoded by this gene is a member of the transmembrane 4 superfamily also known as the tetraspanin family. Most of these members are cell surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development activation growth and motility.