abnormal involuntary movement_Scn1a<tm1Kzy>/Scn1a<tm1Kzy>

http://metadb.riken.jp/0003492I129P2OlaHsdC57BL6Scn1atm1KzyScn1atm1KzyScn1atm1Kzy

abnormal involuntary movement_Scn1a<tm1Kzy>/Scn1a<tm1Kzy>

表現型アノテーション

MGI marker

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

• sodium channel, voltage-gated, type I, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:98246

遺伝子型

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

• Scn1a<tm1Kzy>/Scn1a<tm1Kzy>

アレルシンボル

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

• Scn1a<tm1Kzy>

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

• abnormal involuntary movement
  http://purl.obolibrary.org/obo/MP_0003492

文献

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

• Ikuo. Ogiwara, et.al., Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/17537961