P2Y12 Polyclonal Antibody, 20ul Dry Bath Mutations in this gene are

Mutations in this gene are the cause of hypogonadotropic hypogonadism 20 with or without anosmia

Two transcript variants| one protein-coding and the other non-protein coding| have been found for this gene

Periphilin 1 encoded by PPHLN1 is one of the several proteins that become sequentially incorporated into the cornified cell envelope during the terminal differentiation of keratinocyte at the outer layers of epidermis

The protein encoded by this gene may function as a mediator of the biological consequences of the methylation signal

An important paralog of C1R is HP

P2Y12 Polyclonal Antibody, 20ul Dry Bath Mutations in this gene areThe product of this gene belongs to the family of G protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is involved in platelet aggregation, and is a potential target for the treatment of thromboembolisms and other clotting disorders. Mutations in this gene are implicated in bleeding disorder, platelet