gliosis_Pex13<tm1Crne>/Pex13<tm1.1Crne>,Tg(Nes-cre)1Kln/0

http://metadb.riken.jp/0002183I129T2SvEmsC57BL6C57BL6JSJLPex13tm1CrnePex13tm11CrneTgNescre1Kln0TgNescre1KlnPex13tm1CrnePex13tm11Crne

gliosis_Pex13<tm1Crne>/Pex13<tm1.1Crne>,Tg(Nes-cre)1Kln/0

表現型アノテーション

MGI marker

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

• transgene insertion 1, Rudiger Klein
  http://metadb.riken.jp/db/mgi_rdf/MGI:2176172
• peroxisomal biogenesis factor 13
  http://metadb.riken.jp/db/mgi_rdf/MGI:1919379

遺伝子型

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

• Pex13<tm1Crne>/Pex13<tm1.1Crne>,Tg(Nes-cre)1Kln/0

アレルシンボル

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

• Tg(Nes-cre)1Kln|Pex13<tm1Crne>|Pex13<tm1.1Crne>

遺伝的背景

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

• involves: 129T2/SvEms * C57BL/6 * C57BL/6J * SJL

MP annotation

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

• gliosis
  http://purl.obolibrary.org/obo/MP_0002183

文献

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

• C Catharina. Müller, et.al., PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress., Disease models & mechanisms, 2011, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/20959636