Species Human Entrez 51259 | Human Mouse Ensembl ENSG00000187049 | |
Aliases TMEM216, HSPC244, transmembrane protein 216 External IDs MGI: 1920020 HomoloGene: 9541 GeneCards: TMEM216 | ||
Transmembrane protein 216 is a protein in humans that is encoded by the TMEM216 gene.
Clinical significance
Mutations in this gene may be associated with Meckel syndrome or Joubert syndrome.
References
TMEM216 Wikipedia(Text) CC BY-SA