ABCC7 p.Ser321Ala

CF databases: c.961T>C , p.Ser321Pro (CFTR1) ? , This mutation was identified in one Italian chromosome. No other mutation was identified.
Predicted by SNAP2: A: N (87%), C: D (53%), D: D (71%), E: D (66%), F: D (80%), G: N (53%), H: D (75%), I: D (63%), K: D (80%), L: D (75%), M: D (71%), N: D (59%), P: D (80%), Q: D (71%), R: D (80%), T: N (93%), V: D (66%), W: D (80%), Y: D (80%),
Predicted by PROVEAN: A: N, C: N, D: N, E: N, F: N, G: N, H: N, I: N, K: N, L: N, M: N, N: N, P: N, Q: N, R: N, T: N, V: N, W: N, Y: N,

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[hide] Ge N, Muise CN, Gong X, Linsdell P
Direct comparison of the functional roles played by different transmembrane regions in the cystic fibrosis transmembrane conductance regulator chloride channel pore.
J Biol Chem. 2004 Dec 31;279(53):55283-9. Epub 2004 Oct 25., 2004-12-31 [PMID:15504721]

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