abnormal amino acid level_Slc6a6<tm1Dhau>/Slc6a6<tm1Dhau>

http://metadb.riken.jp/0005332I129X1SvJC57BL6JSlc6a6tm1DhauSlc6a6tm1DhauSlc6a6tm1Dhau

abnormal amino acid level_Slc6a6<tm1Dhau>/Slc6a6<tm1Dhau>

表現型アノテーション

MGI marker

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

• solute carrier family 6 (neurotransmitter transporter, taurine), member 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:98488

遺伝子型

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

• Slc6a6<tm1Dhau>/Slc6a6<tm1Dhau>

アレルシンボル

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

• Slc6a6<tm1Dhau>

遺伝的背景

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

• involves: 129X1/SvJ * C57BL/6J

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

• Birgit. Heller-Stilb, et.al., Disruption of the taurine transporter gene (taut) leads to retinal degeneration in mice., FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2002, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/11772953