delayed endochondral bone ossification_Ror2<tm1Gdy>/Ror2<tm1Gdy>

http://metadb.riken.jp/0003419I129P2OlaHsdRor2tm1GdyRor2tm1GdyRor2tm1Gdy

delayed endochondral bone ossification_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

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

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
• T M. DeChiara, et.al., Ror2, encoding a receptor-like tyrosine kinase, is required for cartilage and growth plate development., Nature genetics, 2000, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/10700181