Gene Review:
AMN - amnion associated transmembrane protein
Homo sapiens
Synonyms:
PRO1028, Protein amnionless, UNQ513/PRO1028, amnionless
- Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in Jordan. Al-Alami, J.R., Tanner, S.M., Tayeh, M.K., de la Chapelle, A., El-Shanti, H. Saudi medical journal. (2005)
- Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria). Gräsbeck, R. Orphanet journal of rare diseases [electronic resource]. (2006)
- Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. Tanner, S.M., Li, Z., Perko, J.D., Oner, C., Cetin, M., Altay, C., Yurtsever, Z., David, K.L., Faivre, L., Ismail, E.A., Gräsbeck, R., de la Chapelle, A. Proc. Natl. Acad. Sci. U.S.A. (2005)
- The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Fyfe, J.C., Madsen, M., Højrup, P., Christensen, E.I., Tanner, S.M., de la Chapelle, A., He, Q., Moestrup, S.K. Blood (2004)