TMEM216 Back

transmembrane protein 216

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NCBI Description of TMEM216

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.

Community Annotation of TMEM216 Add / Edit TMEM216: Annotations

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


TMEM216 is highly significantly mutated in
TMEM216 is significantly mutated in
TMEM216 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for TMEM216