abnormal skeleton development_P2rx7<tm1Gab>/P2rx7<tm1Gab>

http://metadb.riken.jp/0002113EI129P2OlaHsdC57BL6orI129P2OlaHsdC57BL6DBA2P2rx7tm1GabP2rx7tm1GabP2rx7tm1Gab

abnormal skeleton development_P2rx7<tm1Gab>/P2rx7<tm1Gab>

表現型アノテーション

MGI marker

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

• purinergic receptor P2X, ligand-gated ion channel, 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:1339957

遺伝子型

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

• P2rx7<tm1Gab>/P2rx7<tm1Gab>

アレルシンボル

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

• P2rx7<tm1Gab>

遺伝的背景

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

• either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * DBA/2)

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

• Hua Zhu. Ke, et.al., Deletion of the P2X7 nucleotide receptor reveals its regulatory roles in bone formation and resorption., Molecular endocrinology (Baltimore, Md.), 2003, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/12677010