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 D77N 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.
|Cited point mutation:||Asp77Asn|
|General numbering (KChannelDB):||-|
|Other point mutations / same protein||List of mutations in KCNE1_RAT|
IsK related channels (minK,MiRP,AMMECR2)|
Potassium channels 1 TM
|Other point mutations / same position||
Position 76 in IsK related channels (minK,MiRP,AMMECR2) family |
Position 76 in Potassium channels 1 TM family
|Reference:||The long QT syndromes: genetic basis and clinical implications.|
Chiang CE, Roden DM
J Am Coll Cardiol 2000 Jul;36(1):1-12.
|Other point mutations / same article||List|
|Text source||HTML full text|
|Validation status||Not yet checked|