abnormal impulse conducting system conduction_Kcnip2<tm1Krc>/Kcnip2<tm1Krc>

http://metadb.riken.jp/0003137IBlackSwissKcnip2tm1KrcKcnip2tm1KrcKcnip2tm1Krc

abnormal impulse conducting system conduction_Kcnip2<tm1Krc>/Kcnip2<tm1Krc>

表現型アノテーション

MGI marker

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

• Kv channel-interacting protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2135916

遺伝子型

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

• Kcnip2<tm1Krc>/Kcnip2<tm1Krc>

アレルシンボル

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

• Kcnip2<tm1Krc>

遺伝的背景

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

• involves: Black Swiss

MP annotation

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

• abnormal impulse conducting system conduction
  http://purl.obolibrary.org/obo/MP_0003137

文献

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

• H C. Kuo, et.al., A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of I(to) and confers susceptibility to ventricular tachycardia., Cell, 2001, 107
  http://rdf.ncbi.nlm.nih.gov/pubmed/11747815