From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Transmembrane protein 138 is a protein that in humans is encoded by the TMEM138 gene.[5]
Mutations in this gene have been shown to cause a ciliopathy indistinguishable to Joubert syndrome.[6]
- ^ a b c GRCh38: Ensembl release 89: ENSG00000149483 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024666 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Transmembrane protein 138". Retrieved 2012-01-30.
- ^ Lee JH, Silhavy JL, Lee JE, Al-Gazali L, Thomas S, Davis EE, Bielas SL, Hill KJ, Iannicelli M, Brancati F, Gabriel SB, Russ C, Logan CV, Sharif SM, Bennett CP, Abe M, Hildebrandt F, Diplas BH, Attié-Bitach T, Katsanis N, Rajab A, Koul R, Sztriha L, Waters ER, Ferro-Novick S, Woods CG, Johnson CA, Valente EM, Zaki MS, Gleeson JG (Feb 2012). "Evolutionarily assembled cis-regulatory module at a human ciliopathy locus". Science. 335 (6071): 966–9. Bibcode:2012Sci...335..966L. doi:10.1126/science.1213506. PMC 3671610. PMID 22282472.