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 A179T 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||List of mutations in IRK1_HUMAN|
Inward rectifiers (Kir)|
Potassium channels 2 TMs
|Other point mutations / same position||
Position 162 in Inward rectifiers (Kir) family |
Position 162 in Potassium channels 2 TMs family
|Reference:||Functional implications of mutations in the human renal outer medullary potassium channel (ROMK2) identified in Bartter syndrome.|
Starremans PG, van der Kemp AW, Knoers NV, van den Heuvel LP, Bindels RJ
Pflugers Arch 2002 Jan;443(3):466-72.
|Other point mutations / same article||List|
|Validation status||Not yet checked|