This data was extracted from Medline abstracts and full texts (when available) in an automated manner.
The table below describes the selected point mutation and provides links to other documents. The sentence(s) where the point mutation D85N was found are listed after the table.
The mutated residues are also indicated in the family sequence alignments and hyperlinked to the corresponding mutation pages.
|General numbering (KChannelDB):||-|
|Other point mutations / same protein / same position||Point mutations at position 85 in KCNE1_HUMAN|
|Other point mutations / same protein||List of mutations in KCNE1_HUMAN|
IsK related channels (minK,MiRP,AMMECR2)|
Potassium channels 1 TM
|Other point mutations / same position||
Position 85 in IsK related channels (minK,MiRP,AMMECR2) family |
Position 85 in Potassium channels 1 TM family
|Reference:||Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.|
Paulussen AD, Gilissen RA, Armstrong M, Doevendans PA, Verhasselt P, Smeets HJ, Schulze-Bahr E, Haverkamp W, Breithardt G, Cohen N, Aerssens J
J Mol Med 2004 Mar;82(3):182-8. Epub 2004 Feb 4.
|Other point mutations / same article||List|
|Validation status||Not yet checked|