abnormal circulating phospholipid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>

http://metadb.riken.jp/0006084I129C57BL6NPex1tm11SjmsPex1tm11SjmsPex1tm11Sjms

abnormal circulating phospholipid level_Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>

表現型アノテーション

MGI marker

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

• peroxisomal biogenesis factor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1918632

遺伝子型

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

• Pex1<tm1.1Sjms>/Pex1<tm1.1Sjms>

アレルシンボル

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

• Pex1<tm1.1Sjms>

遺伝的背景

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

• involves: 129 * C57BL/6N

MP annotation

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

• abnormal circulating phospholipid level
  http://purl.obolibrary.org/obo/MP_0006084

文献

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

• 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