no abnormal phenotype detected_Slc48a1<Gt(U3Betageo)1Ruiz>/Slc48a1<Gt(U3Betageo)1Ruiz>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6Slc48a1GtU3Betageo1RuizSlc48a1GtU3Betageo1RuizSlc48a1GtU3Betageo1Ruiz

no abnormal phenotype detected_Slc48a1<Gt(U3Betageo)1Ruiz>/Slc48a1<Gt(U3Betageo)1Ruiz>

表現型アノテーション

MGI marker

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

• solute carrier family 48 (heme transporter), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1914989

遺伝子型

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

• Slc48a1<Gt(U3Betageo)1Ruiz>/Slc48a1<Gt(U3Betageo)1Ruiz>

アレルシンボル

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

• Slc48a1<Gt(U3Betageo)1Ruiz>

遺伝的背景

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

• involves: 129S2/SvPas * 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

• Jens. Hansen, et.al., A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome., Proceedings of the National Academy of Sciences of the United States of America, 2003, 100
  http://rdf.ncbi.nlm.nih.gov/pubmed/12904583