polydactyly_Del(2Hoxd11-Hoxd13)29Ddu/Del(2Hoxd11-Hoxd13)29Ddu

http://metadb.riken.jp/0000562I129S2SvPasDel2Hoxd11Hoxd1329DduDel2Hoxd11Hoxd1329DduDel2Hoxd11Hoxd1329Ddu

polydactyly_Del(2Hoxd11-Hoxd13)29Ddu/Del(2Hoxd11-Hoxd13)29Ddu

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 29
  http://metadb.riken.jp/db/mgi_rdf/MGI:3762254

遺伝子型

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

• Del(2Hoxd11-Hoxd13)29Ddu/Del(2Hoxd11-Hoxd13)29Ddu

アレルシンボル

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

• Del(2Hoxd11-Hoxd13)29Ddu

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

• polydactyly
  http://purl.obolibrary.org/obo/MP_0000562

文献

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

• Olivier. Cocquempot, et.al., Fork stalling and template switching as a mechanism for polyalanine tract expansion affecting the DYC mutant of HOXD13, a new murine model of synpolydactyly., Genetics, 2009, 183
  http://rdf.ncbi.nlm.nih.gov/pubmed/19546318
• S. Bruneau, et.al., The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes., Developmental biology, 2001, 237
  http://rdf.ncbi.nlm.nih.gov/pubmed/11543619
• J. Zákány, et.al., Synpolydactyly in mice with a targeted deficiency in the HoxD complex., Nature, 1996, 384
  http://rdf.ncbi.nlm.nih.gov/pubmed/8900279