TMEM216

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VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

n/a

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

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

  1. "Entrez Gene: transmembrane protein 216".
  2. Wang A (September 2010). "TMEM216 joins its ciliary cousins in ciliopathies". Clin Genet. 79 (1): 45–7. doi:10.1111/j.1399-0004.2010.01556_2.x. PMID 21029074.

Further reading



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