KChannelDB: Point mutations extracted from the literature - IRK6_HUMAN

2005, KChannelDB.

This data was extracted from medline abstracts and full text papers (when available) in an automated manner.

Each point mutation is linked to the entry specific to the residue position. Citations are linked to the list of point mutations found in the corresponding articles. The last column allows you to go back to the original text via Medline.

Protein	IRK6_HUMAN (KCNJ6,GIRK2, KATP2, KCNJ)	Swiss-Prot Cross-reference table Family page
Family alignments	Inward rectifiers (Kir) Potassium channels 2 TMs

Mutation Location General numbering Reference
D79N N-term Kuzhikandathil EV et al., J Gen Physiol 2000 Medline

G156S Loop 1-2 Kuzhikandathil EV et al., J Gen Physiol 2000 Medline

L220F C-term Lopes CM et al., Neuron 2002 Medline

Mutation	Location	Reference
D79N	N-term	Kuzhikandathil EV et al., J Gen Physiol 2000	Medline
G156S	Loop 1-2	Kuzhikandathil EV et al., J Gen Physiol 2000	Medline
L220F	C-term	Lopes CM et al., Neuron 2002	Medline

F.Horn (kchanneldbcmbi.ru.nl), 17-Aug-2005