anemia_Fn1<tm4Hyn>/Fn1<tm4Hyn>

http://metadb.riken.jp/0001577I129P2OlaHsdC57BL6JFn1tm4HynFn1tm4HynFn1tm4Hyn

anemia_Fn1<tm4Hyn>/Fn1<tm4Hyn>

表現型アノテーション

MGI marker

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

• fibronectin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95566

遺伝子型

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

• Fn1<tm4Hyn>/Fn1<tm4Hyn>

アレルシンボル

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

• Fn1<tm4Hyn>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6J

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• anemia
  http://purl.obolibrary.org/obo/MP_0001577

文献

http://purl.org/net/cito/citesAsAuthority

• Sophie. Astrof, et.al., Multiple cardiovascular defects caused by the absence of alternatively spliced segments of fibronectin., Developmental biology, 2007, 311
  http://rdf.ncbi.nlm.nih.gov/pubmed/17706958