hindlimb paralysis_Del(2Hoxd10)13Ddu/Del(2Hoxd10)13Ddu

http://metadb.riken.jp/0000755I129S2SvPasDel2Hoxd1013DduDel2Hoxd1013DduDel2Hoxd1013Ddu

hindlimb paralysis_Del(2Hoxd10)13Ddu/Del(2Hoxd10)13Ddu

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 13
  http://metadb.riken.jp/db/mgi_rdf/MGI:3616193

遺伝子型

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

• Del(2Hoxd10)13Ddu/Del(2Hoxd10)13Ddu

アレルシンボル

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

• Del(2Hoxd10)13Ddu

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

• hindlimb paralysis
  http://purl.obolibrary.org/obo/MP_0000755

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