Species Human Entrez 51524 | Human Mouse Ensembl ENSG00000149483 | |
Aliases TMEM138, HSPC196, transmembrane protein 138 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