TMEM216
From Infogalactic: the planetary knowledge core
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Transmembrane protein 216 is a protein in humans that is encoded by the TMEM216 gene.[1]
Clinical significance
Mutations in this gene may be associated with Meckel syndrome or Joubert syndrome.[2]
See also
References
Further reading
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