no abnormal phenotype detected_Dmd<Gt(pT1ATGBetageo)1Ruiz>/Dmd<Gt(pT1ATGBetageo)1Ruiz>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6DmdGtpT1ATGBetageo1RuizDmdGtpT1ATGBetageo1RuizDmdGtpT1ATGBetageo1Ruiz

no abnormal phenotype detected_Dmd<Gt(pT1ATGBetageo)1Ruiz>/Dmd<Gt(pT1ATGBetageo)1Ruiz>

表現型アノテーション

MGI marker

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

• dystrophin, muscular dystrophy
  http://metadb.riken.jp/db/mgi_rdf/MGI:94909

遺伝子型

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

• Dmd<Gt(pT1ATGBetageo)1Ruiz>/Dmd<Gt(pT1ATGBetageo)1Ruiz>

アレルシンボル

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

• Dmd<Gt(pT1ATGBetageo)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