aminoaciduria_Slc22a5<jvs>/Slc22a5<jvs>

http://metadb.riken.jp/0003311C3OHH2o2Slc22a5jvsSlc22a5jvsSlc22a5jvsSlc22a5jvs

aminoaciduria_Slc22a5<jvs>/Slc22a5<jvs>

表現型アノテーション

MGI marker

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

• solute carrier family 22 (organic cation transporter), member 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:1329012

遺伝子型

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

• Slc22a5<jvs>/Slc22a5<jvs>

アレルシンボル

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

• Slc22a5<jvs>

遺伝的背景

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

• C3.OH-H2<o2> Slc22a5<jvs>

MP annotation

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

• aminoaciduria
  http://purl.obolibrary.org/obo/MP_0003311

文献

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

• M. Horiuchi, et.al., Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system., Biochimica et biophysica acta, 1994, 1226
  http://rdf.ncbi.nlm.nih.gov/pubmed/8155735