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 D79N 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):||-|
|Protein:||IRK6_HUMAN (KCNJ6,GIRK2, KATP2, KCNJ)||Swiss-Prot|
|Other point mutations / same protein||List of mutations in IRK6_HUMAN|
Inward rectifiers (Kir)|
Potassium channels 2 TMs
|Other point mutations / same position||
Position 50 in Inward rectifiers (Kir) family |
Position 50 in Potassium channels 2 TMs family
|Reference:||Dominant-negative mutants identify a role for GIRK channels in D3 dopamine receptor-mediated regulation of spontaneous secretory activity.|
Kuzhikandathil EV, Oxford GS
J Gen Physiol 2000 Jun;115(6):697-706.
|Other point mutations / same article||List|
|Text source||HTML full text|
|Validation status||Not yet checked|