ANO10 Polyclonal Antibody, 50ul Centrifuge Tube (Bottle) Mutations in CUBN may play

Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia

Naturally occurring readthrough transcription occurs between this locus and downstream LOC100130357

MIM 601974) are S1P receptors

miscellaneous:The EU sequence has the INV (3) allotypic marker| Ala-45 and Val-83

It is not known if these transcripts are translated| or if the possible protein product provides any functional role

ANO10 Polyclonal Antibody, 50ul Centrifuge Tube (Bottle) Mutations in CUBN may playThe transmembrane protein encoded by this gene is a member of a family of calcium activated chloride channels. Defects in this gene may be a cause of autosomal recessive spinocerebellar ataxia 10. Several transcript variants encoding different isoforms have been found for this gene.