hypotonia_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>

http://metadb.riken.jp/0004144I129T2SvEmsC57BL6JPex13tm11CrnePex13tm11CrnePex13tm11Crne

hypotonia_Pex13<tm1.1Crne>/Pex13<tm1.1Crne>

表現型アノテーション

MGI marker

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

• 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<tm1.1Crne>/Pex13<tm1.1Crne>

アレルシンボル

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

• Pex13<tm1.1Crne>

遺伝的背景

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

• involves: 129T2/SvEms * C57BL/6J

MP annotation

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

• hypotonia
  http://purl.obolibrary.org/obo/MP_0004144

文献

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

• Megan. Maxwell, et.al., Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype., Molecular and cellular biology, 2003, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/12897163