P L. Faust, et.al., Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder., The Journal of cell biology, 1997, 139

http://rdf.ncbi.nlm.nih.gov/pubmed/9382874

P L. Faust, et.al., Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder., The Journal of cell biology, 1997, 139

pubmed

allele

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

• Pex2<tm1Plf>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2180128

表現型アノテーション

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

• abnormal interparietal bone morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000077I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal stratification in cerebral cortex_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000790I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal motor capabilities/coordination/movement_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0002066I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal frontal bone morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000107I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal liver morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000598I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• hypoactivity_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0001402I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• delayed intramembranous bone ossification_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0003420I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• trunk curl_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0001512I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal neurocranium morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000074I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• neonatal lethality, incomplete penetrance_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0011088I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• decreased bone mineralization_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0020137I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• decreased bone mineral density_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000063I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• impaired balance_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0001525I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal head movements_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0000436I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal circulating free fatty acids level_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0001553I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal brain white matter morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0008026I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• aphagia_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0001438I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• decreased embryo weight_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0009429I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• abnormal adrenal cortex morphology_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0008288I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf
• postnatal lethality, complete penetrance_Pex2<tm1Plf>/Pex2<tm1Plf>
  http://metadb.riken.jp/0011085I129S1Sv129X1SvJC57BL6Pex2tm1PlfPex2tm1PlfPex2tm1Plf

class

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

• Pex2<tm1Plf>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2180128

トランスクリプトームデータ

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

• CD02560
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD02560