muscular atrophy_Tg(Thy1-BSCL2*N88S)#Dit/0

http://metadb.riken.jp/0002269IC57BL6DBA2TgThy1BSCL2N88SDit0TgThy1BSCL2N88SDit

muscular atrophy_Tg(Thy1-BSCL2*N88S)#Dit/0

表現型アノテーション

MGI marker

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

• transgene insertion, Daisuke Ito
  http://metadb.riken.jp/db/mgi_rdf/MGI:5295190

遺伝子型

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

• Tg(Thy1-BSCL2*N88S)#Dit/0

アレルシンボル

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

• Tg(Thy1-BSCL2*N88S)#Dit

遺伝的背景

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

• involves: C57BL/6 * DBA/2

MP annotation

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

• muscular atrophy
  http://purl.obolibrary.org/obo/MP_0002269

文献

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

• Takuya. Yagi, et.al., N88S seipin mutant transgenic mice develop features of seipinopathy/BSCL2-related motor neuron disease via endoplasmic reticulum stress., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21750110