short nasal bone_Ror2<tm1Gdy>/Ror2<tm1Gdy>

http://metadb.riken.jp/0004471I129P2OlaHsdRor2tm1GdyRor2tm1GdyRor2tm1Gdy

short nasal bone_Ror2<tm1Gdy>/Ror2<tm1Gdy>

表現型アノテーション

MGI marker

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

• receptor tyrosine kinase-like orphan receptor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347521

遺伝子型

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

• Ror2<tm1Gdy>/Ror2<tm1Gdy>

アレルシンボル

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

• Ror2<tm1Gdy>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• short nasal bone
  http://purl.obolibrary.org/obo/MP_0004471

文献

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

• Regina. Raz, et.al., The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome., Development (Cambridge, England), 2008, 135
  http://rdf.ncbi.nlm.nih.gov/pubmed/18353862