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

http://metadb.riken.jp/0003419B6C3FeaaHoxd13spdhJHoxd13spdhHoxd13spdhHoxd13spdh

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

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<spdh>

アレルシンボル

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

• Hoxd13<spdh>

遺伝的背景

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

• B6C3Fe a/a-Hoxd13<spdh>/J

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