abnormal lipid homeostasis_Ehhadh<tm1Jkr>/Ehhadh<tm1Jkr>

http://metadb.riken.jp/0002118I129P2OlaHsdC57BL6JEhhadhtm1JkrEhhadhtm1JkrEhhadhtm1Jkr

abnormal lipid homeostasis_Ehhadh<tm1Jkr>/Ehhadh<tm1Jkr>

表現型アノテーション

MGI marker

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

• enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1277964

遺伝子型

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

• Ehhadh<tm1Jkr>/Ehhadh<tm1Jkr>

アレルシンボル

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

• Ehhadh<tm1Jkr>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• abnormal lipid homeostasis
  http://purl.obolibrary.org/obo/MP_0002118

文献

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

• M. Baes, et.al., The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation., Journal of neuropathology and experimental neurology, 2002, 61
  http://rdf.ncbi.nlm.nih.gov/pubmed/11939592