KChannelDB: Point mutations extracted from the literature - Q86W40_HUMAN

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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.


ProteinQ86W40_HUMAN (KCNQ5,RP11-257K9.5-00)Swiss-Prot
Cross-reference table
Family page
Family alignments KQT related KCNQ (Kv7)
K+ voltage-gated channels (Kv1-12,Kca2-5)
Potassium channels 6 TMs

MutationLocationGeneral numberingReference
P2XN-term Robbins et al., Pharmacol Ther 2001Medline
A212ELoop 3-4 Robbins et al., Pharmacol Ther 2001Medline
A212VLoop 3-4 Robbins et al., Pharmacol Ther 2001Medline


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