delayed endochondral bone ossification_Hoxd13<spdh>/Hoxd13<tm1Ddu>

http://metadb.riken.jp/0003419I129S2SvPasC3HeBFeJLeC57BL6JHoxd13spdhHoxd13tm1DduHoxd13tm1DduHoxd13spdh

delayed endochondral bone ossification_Hoxd13<spdh>/Hoxd13<tm1Ddu>

表現型アノテーション

MGI marker

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

• homeobox D13
  http://metadb.riken.jp/db/mgi_rdf/MGI:96205

遺伝子型

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

• Hoxd13<spdh>/Hoxd13<tm1Ddu>

アレルシンボル

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

• Hoxd13<tm1Ddu>|Hoxd13<spdh>

遺伝的背景

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

• involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• delayed endochondral bone ossification
  http://purl.obolibrary.org/obo/MP_0003419

文献

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

• 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