Entrez 51524 | Ensembl ENSG00000149483 | |
External IDs MGI: 1920232 HomoloGene: 9518 GeneCards: TMEM138 |
Transmembrane protein 138 is a protein that in humans is encoded by the TMEM138 gene.
Clinical relevance
Mutations in this gene have been shown to cause a ciliopathy indistinguishable to Joubert syndrome.
References
TMEM138 Wikipedia(Text) CC BY-SA