KChannelDB: Extraction of mutation data from the literature

logo    2005, KChannelDB.


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 G628C 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.


Point mutation G628C in KCNH2_HUMAN

Point mutation:G628C
Domain:Loop 5-6
General numbering (KChannelDB): -
Protein:KCNH2_HUMAN (KCNH2,ERG, ERG1, HERG, HERG)Swiss-Prot
Cross-reference table
Family page
Protein isoforms4
Other point mutations / same protein / same positionPoint mutations at position 628 in KCNH2_HUMAN
Other point mutations / same proteinList of mutations in KCNH2_HUMAN
Family alignments eag related KCNH (Kv10-12)
K+ voltage-gated channels (Kv1-12,Kca2-5)
Potassium channels 6 TMs
Other point mutations / same position Position 628 in eag related KCNH (Kv10-12) family
Position 616 in K+ voltage-gated channels (Kv1-12,Kca2-5) family
Position 376 in Potassium channels 6 TMs family
Reference:Open channel block of HERG K(+) channels by vesnarinone.
Kamiya K, Mitcheson JS, Yasui K, Kodama I, Sanguinetti MC
Mol Pharmacol 2001 Aug;60(2):244-53.
Medline
Other point mutations / same articleList
Text sourceHTML full text
Validation statusNot yet checked

Relevant sentences:

G628C


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