Pedro. Brites, et.al., Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata., Human molecular genetics, 2003, 12

http://rdf.ncbi.nlm.nih.gov/pubmed/12915479

Pedro. Brites, et.al., Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata., Human molecular genetics, 2003, 12

pubmed

allele

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

• Pex7<tm1Rjaw>
  http://metadb.riken.jp/db/mgi_rdf/MGI:3052739

class

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

• Pex7<tm1Rjaw>
  http://metadb.riken.jp/db/mgi_rdf/MGI:3052739

表現型アノテーション

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

• neonatal lethality, incomplete penetrance_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0011088SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• dystonia_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0005323SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• infertility_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0001924SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• testicular atrophy_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0003205SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal neuronal migration_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0006009SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal lipid level_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0001547SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal osteoclast morphology_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0004982SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal eating behavior_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0001431SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• increased fatty acid level_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0005281SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• decreased body weight_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0001262SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal cerebral cortex morphology_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0000788SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• decreased bone mineralization_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0020137SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• abnormal cartilage development_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0000164SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• cataract_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0001304SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw
• disproportionate dwarf_Pex7<tm1Rjaw>/Pex7<tm1Rjaw>
  http://metadb.riken.jp/0002427SwissPex7tm1RjawPex7tm1RjawPex7tm1Rjaw

トランスクリプトームデータ

http://rdf.ncbi.nlm.nih.gov/pubmed/

• CD04942
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD04942
• CD48029
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD48029