muscular atrophy_Del(2Hoxd9-Hoxd13)8Ddu/Del(2Hoxd9-Hoxd13)8Ddu

http://metadb.riken.jp/0002269I129S2SvPasDel2Hoxd9Hoxd138DduDel2Hoxd9Hoxd138DduDel2Hoxd9Hoxd138Ddu

muscular atrophy_Del(2Hoxd9-Hoxd13)8Ddu/Del(2Hoxd9-Hoxd13)8Ddu

表現型アノテーション

MGI marker

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

• deletion, Chr 2, Denis Duboule 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:3616162

遺伝子型

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

• Del(2Hoxd9-Hoxd13)8Ddu/Del(2Hoxd9-Hoxd13)8Ddu

アレルシンボル

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

• Del(2Hoxd9-Hoxd13)8Ddu

遺伝的背景

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

• involves: 129S2/SvPas

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

• Basile. Tarchini, et.al., HoxD cluster scanning deletions identify multiple defects leading to paralysis in the mouse mutant Ironside., Genes & development, 2005, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/16322559