no abnormal phenotype detected_Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>

http://metadb.riken.jp/0002169I129C57BL6Hsd17b4tm2BaesHsd17b4tm2BaesHsd17b4tm2Baes

no abnormal phenotype detected_Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>

表現型アノテーション

MGI marker

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

• hydroxysteroid (17-beta) dehydrogenase 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:105089

遺伝子型

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

• Hsd17b4<tm2Baes>/Hsd17b4<tm2Baes>

アレルシンボル

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

• Hsd17b4<tm2Baes>

遺伝的背景

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

• involves: 129 * C57BL/6

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Simon. Verheijden, et.al., Peroxisomal multifunctional protein-2 deficiency causes neuroinflammation and degeneration of Purkinje cells independent of very long chain fatty acid accumulation., Neurobiology of disease, 2013, 58
  http://rdf.ncbi.nlm.nih.gov/pubmed/23777740