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This locus encodes a transmembrane domain-containing protein. Additionally we are shipping and many more products for this protein.
study reports that mutation of either TMEM138 (show TMEM138 ELISA Kits) or TMEM216 causes a phenotypically indistinguishable ciliopathy, Joubert syndrome; expression of the genes is mediated by a conserved regulatory element in the noncoding intergenic region
a TMEM216 mutation may have a role in Joubert syndrome 2 (JBTS2) in Ashkenazi Jews
This locus encodes a transmembrane domain-containing protein. Mutations at this locus have been associated with Meckel-Gruber Syndrome Type 2, and Joubert Syndrome 2, also known as Cerebello-oculorenal Syndrome 2.
transmembrane protein 216
, thymus atrophy-related protein