abnormal amino acid level_Slc7a10<tm1Dgen>/Slc7a10<tm1Dgen>

http://metadb.riken.jp/0005332I129P2OlaHsdC57BL6Slc7a10tm1DgenSlc7a10tm1DgenSlc7a10tm1Dgen

abnormal amino acid level_Slc7a10<tm1Dgen>/Slc7a10<tm1Dgen>

表現型アノテーション

MGI marker

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

• solute carrier family 7 (cationic amino acid transporter, y+ system), member 10
  http://metadb.riken.jp/db/mgi_rdf/MGI:1858261

遺伝子型

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

• Slc7a10<tm1Dgen>/Slc7a10<tm1Dgen>

アレルシンボル

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

• Slc7a10<tm1Dgen>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal amino acid level
  http://purl.obolibrary.org/obo/MP_0005332

文献

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

• A Richard. Rutter, et.al., Evidence from gene knockout studies implicates Asc-1 as the primary transporter mediating d-serine reuptake in the mouse CNS., The European journal of neuroscience, 2007, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/17432963