abnormal skeleton development_Mmp2<tm1Ito>/Mmp2<tm1Ito>

http://metadb.riken.jp/0002113I129P2OlaHsdMmp2tm1ItoMmp2tm1ItoMmp2tm1Ito

abnormal skeleton development_Mmp2<tm1Ito>/Mmp2<tm1Ito>

表現型アノテーション

MGI marker

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

• matrix metallopeptidase 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97009

遺伝子型

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

• Mmp2<tm1Ito>/Mmp2<tm1Ito>

アレルシンボル

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

• Mmp2<tm1Ito>

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

• abnormal skeleton development
  http://purl.obolibrary.org/obo/MP_0002113

文献

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

• Rebecca A. Mosig, et.al., Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth., Human molecular genetics, 2007, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/17400654