Gene Review:
TMC2 - transmembrane channel-like 2
Homo sapiens
Synonyms:
C20orf145, Transmembrane channel-like protein 2, Transmembrane cochlear-expressed protein 2, UNQ907/PRO1928, dJ686C3.3
- Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Kurima, K., Peters, L.M., Yang, Y., Riazuddin, S., Ahmed, Z.M., Naz, S., Arnaud, D., Drury, S., Mo, J., Makishima, T., Ghosh, M., Menon, P.S., Deshmukh, D., Oddoux, C., Ostrer, H., Khan, S., Riazuddin, S., Deininger, P.L., Hampton, L.L., Sullivan, S.L., Battey, J.F., Keats, B.J., Wilcox, E.R., Friedman, T.B., Griffith, A.J. Nat. Genet. (2002)
- Dipeptidyl peptidase IV on activated T cells as a target molecule for therapy of rheumatoid arthritis. Williams, Y.N., Baba, H., Hayashi, S., Ikai, H., Sugita, T., Tanaka, S., Miyasaka, N., Kubota, T. Clin. Exp. Immunol. (2003)