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This gene is expressed exclusively in the brain

The solute carrier family 39 member 2 functions as a zinc transporter

Mutations in these genes have been associated with White Sponge Nevus

Mutations in KAL1 cause the X-linked Kallmann syndrome

S2P Polyclonal Antibody, 100ul Immune Cell Analysis Take your research to newMBTPS2 (membrane bound transcription factor peptidase, site 2) encodes a intramembrane zinc metalloprotease, which is essential in development. This protease functions in the signal protein activation involved in sterol control of transcription and the ER stress response. Mutations in MBTPS2 have been associated with ichthyosis follicularis with atrichia and photophobia (IFAP syndrome); IFAP syndrome has been quantitatively linked to a reduction in