muscular atrophy_Tg(SOD1*G37R)42Dpr/0

http://metadb.riken.jp/0002269IC3HHeJC57BL6JTgSOD1G37R42Dpr0TgSOD1G37R42Dpr

muscular atrophy_Tg(SOD1*G37R)42Dpr/0

表現型アノテーション

MGI marker

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

• transgene insertion 42, Donald L Price
  http://metadb.riken.jp/db/mgi_rdf/MGI:3573957

遺伝子型

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

• Tg(SOD1*G37R)42Dpr/0

アレルシンボル

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

• Tg(SOD1*G37R)42Dpr

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6J

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

• P C. Wong, et.al., An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria., Neuron, 1995, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/7605627