Shandi. Hiebler, et.al., The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder., Molecular genetics and metabolism, 2014, 111

http://rdf.ncbi.nlm.nih.gov/pubmed/24503136

Shandi. Hiebler, et.al., The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorder., Molecular genetics and metabolism, 2014, 111

pubmed

allele

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

• Pex1<tm1.2Sjms>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5822916
• Pex1<tm1.1Sjms>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5570186

表現型アノテーション

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

• increased fatty acid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0005281I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal retinal rod cell outer segment morphology_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0008456I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• decreased fatty acid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0005282I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• postnatal growth retardation_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0001732I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• retinal cone cell degeneration_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0008444I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• increased saturated fatty acid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0005284I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal circulating phospholipid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0006084I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• premature death_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0002083I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal bile salt homeostasis_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0005365I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• hepatic steatosis_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0002628I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal cone electrophysiology_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0004022I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal rod electrophysiology_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0004021I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• bile duct proliferation_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0003255I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• cholestasis_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0000610I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• abnormal intestinal lipid absorption_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0005342I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms
• decreased body weight_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>
  http://metadb.riken.jp/0001262I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms

class

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

• Pex1<tm1.2Sjms>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5822916
• Pex1<tm1.1Sjms>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5570186