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TMEM216

Official Full Name
transmembrane protein 216
Organism
Homo sapiens
GeneID
51259
Background
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. [provided by RefSeq, Aug 2010]
Synonyms
RP98; HSPC244;

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