no abnormal phenotype detected_Smad2<tm1.1Mwst>/Smad2<tm1.2Mwst>

http://metadb.riken.jp/0002169I129S6SvEvTacBlackSwissSmad2tm11MwstSmad2tm12MwstSmad2tm11MwstSmad2tm12Mwst

no abnormal phenotype detected_Smad2<tm1.1Mwst>/Smad2<tm1.2Mwst>

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<tm1.1Mwst>/Smad2<tm1.2Mwst>

アレルシンボル

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

• Smad2<tm1.1Mwst>|Smad2<tm1.2Mwst>

遺伝的背景

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

• involves: 129S6/SvEvTac * Black Swiss

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

• Ye. Liu, et.al., Generation of novel conditional and hypomorphic alleles of the Smad2 gene., Genesis (New York, N.Y. : 2000), 2004, 40
  http://rdf.ncbi.nlm.nih.gov/pubmed/15452874