abnormal locomotor activation_Snca<tm1.1Koks>/Snca<+>

http://metadb.riken.jp/0003313EB6129P2Sncatm11KoksorI129P2OlaHsdC57BL6Sncatm11KoksSncaSncatm11KoksSnca

abnormal locomotor activation_Snca<tm1.1Koks>/Snca<+>

表現型アノテーション

MGI marker

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

• synuclein, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:1277151

遺伝子型

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

• Snca<tm1.1Koks>/Snca<+>

アレルシンボル

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

• Snca<tm1.1Koks>|Snca<+>

遺伝的背景

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

• either: B6.129P2-Snca<tm1.1Koks> or (involves: 129P2/OlaHsd * C57BL/6)

MP annotation

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

• abnormal locomotor activation
  http://purl.obolibrary.org/obo/MP_0003313

文献

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

• M. Plaas, et.al., Alpha-synuclein A30P point-mutation generates age-dependent nigrostriatal deficiency in mice., Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 2008, 59
  http://rdf.ncbi.nlm.nih.gov/pubmed/18622040