TMEM138
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 138 is a protein that in humans is encoded by the TMEM138 gene.[1]
Clinical relevance
Mutations in this gene have been shown to cause a ciliopathy indistinguishable to Joubert syndrome.[2]
References
Further reading
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