no abnormal phenotype detected_Tg(Prnp-SNCA)20Vle/0

http://metadb.riken.jp/0002169IC3HC57BL6TgPrnpSNCA20Vle0TgPrnpSNCA20Vle

no abnormal phenotype detected_Tg(Prnp-SNCA)20Vle/0

表現型アノテーション

MGI marker

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

• transgene insertion 20, Virginia M-Y Lee
  http://metadb.riken.jp/db/mgi_rdf/MGI:3574076

遺伝子型

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

• Tg(Prnp-SNCA)20Vle/0

アレルシンボル

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

• Tg(Prnp-SNCA)20Vle

遺伝的背景

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

• involves: C3H * C57BL/6

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Benoit I. Giasson, et.al., Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein., Neuron, 2002, 34
  http://rdf.ncbi.nlm.nih.gov/pubmed/12062037