hyperlipidemia_Slc52a3<tm2a(KOMP)Wtsi>/Slc52a3<tm2a(KOMP)Wtsi>

http://metadb.riken.jp/0001548IC57BL6NSlc52a3tm2aKOMPWtsiSlc52a3tm2aKOMPWtsiSlc52a3tm2aKOMPWtsi

hyperlipidemia_Slc52a3<tm2a(KOMP)Wtsi>/Slc52a3<tm2a(KOMP)Wtsi>

表現型アノテーション

MGI marker

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

• solute carrier protein family 52, member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1916948

遺伝子型

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

• Slc52a3<tm2a(KOMP)Wtsi>/Slc52a3<tm2a(KOMP)Wtsi>

アレルシンボル

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

• Slc52a3<tm2a(KOMP)Wtsi>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• hyperlipidemia
  http://purl.obolibrary.org/obo/MP_0001548

文献

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

• Hiroki. Yoshimatsu, et.al., Disruption of Slc52a3 gene causes neonatal lethality with riboflavin deficiency in mice., Scientific reports, 2016, 6
  http://rdf.ncbi.nlm.nih.gov/pubmed/27272163