no abnormal phenotype detected_Smad2<m1Mag>/Smad2<+>

http://metadb.riken.jp/0002169EI129SSvBlackSwissorI129SSvC57BL6Smad2m1MagSmad2Smad2Smad2m1Mag

no abnormal phenotype detected_Smad2<m1Mag>/Smad2<+>

表現型アノテーション

MGI marker

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

• SMAD family member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:108051

遺伝子型

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

• Smad2<m1Mag>/Smad2<+>

アレルシンボル

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

• Smad2<+>|Smad2<m1Mag>

遺伝的背景

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

• either: (involves: 129S/Sv * Black Swiss) or (involves: 129S/Sv * 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

• Jay L. Vivian, et.al., An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells., Proceedings of the National Academy of Sciences of the United States of America, 2002, 99
  http://rdf.ncbi.nlm.nih.gov/pubmed/12432092