utricular macular degeneration_Kcnq1<tm1Apf>/Kcnq1<tm1Apf>

http://metadb.riken.jp/0004334I129P2OlaHsdC57BL6Kcnq1tm1ApfKcnq1tm1ApfKcnq1tm1Apf

utricular macular degeneration_Kcnq1<tm1Apf>/Kcnq1<tm1Apf>

表現型アノテーション

MGI marker

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

• potassium voltage-gated channel, subfamily Q, member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:108083

遺伝子型

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

• Kcnq1<tm1Apf>/Kcnq1<tm1Apf>

アレルシンボル

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

• Kcnq1<tm1Apf>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• utricular macular degeneration
  http://purl.obolibrary.org/obo/MP_0004334

文献

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

• Alejandro. Rivas, et.al., Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome., Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 2005, 26
  http://rdf.ncbi.nlm.nih.gov/pubmed/15891643