hypokalemia_Kcnk3<tm1.1Daba>/Kcnk3<tm1.1Daba>,Kcnk9<tm1.1Daba>/Kcnk9<tm1.1Daba>

http://metadb.riken.jp/0004119I129S1Sv129X1SvJC57BL6CBAKcnk3tm11DabaKcnk3tm11DabaKcnk9tm11DabaKcnk9tm11DabaKcnk9tm11DabaKcnk3tm11Daba

hypokalemia_Kcnk3<tm1.1Daba>/Kcnk3<tm1.1Daba>,Kcnk9<tm1.1Daba>/Kcnk9<tm1.1Daba>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• potassium channel, subfamily K, member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1100509
• potassium channel, subfamily K, member 9
  http://metadb.riken.jp/db/mgi_rdf/MGI:3521816

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Kcnk3<tm1.1Daba>/Kcnk3<tm1.1Daba>,Kcnk9<tm1.1Daba>/Kcnk9<tm1.1Daba>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Kcnk9<tm1.1Daba>|Kcnk3<tm1.1Daba>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• hypokalemia
  http://purl.obolibrary.org/obo/MP_0004119

文献

http://purl.org/net/cito/citesAsAuthority

• Lucinda A. Davies, et.al., TASK channel deletion in mice causes primary hyperaldosteronism., Proceedings of the National Academy of Sciences of the United States of America, 2008, 105
  http://rdf.ncbi.nlm.nih.gov/pubmed/18250325