no abnormal phenotype detected_Tg(SOD1*A4V)A1073Gur/0

http://metadb.riken.jp/0002169IC57BL6SJLTgSOD1A4VA1073Gur0TgSOD1A4VA1073Gur

no abnormal phenotype detected_Tg(SOD1*A4V)A1073Gur/0

表現型アノテーション

MGI marker

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

• transgene insertion A1073, Mark E Gurney
  http://metadb.riken.jp/db/mgi_rdf/MGI:5449882

遺伝子型

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

• Tg(SOD1*A4V)A1073Gur/0

アレルシンボル

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

• Tg(SOD1*A4V)A1073Gur

遺伝的背景

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

• involves: C57BL/6 * SJL

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

• M E. Gurney, et.al., Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation., Science (New York, N.Y.), 1994, 264
  http://rdf.ncbi.nlm.nih.gov/pubmed/8209258
• Han-Xiang. Deng, et.al., Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria., Proceedings of the National Academy of Sciences of the United States of America, 2006, 103
  http://rdf.ncbi.nlm.nih.gov/pubmed/16636275