absent vitelline blood vessels_Foxo1<tm1Whb>/Foxo1<tm1Whb>

http://metadb.riken.jp/0001719NSFoxo1tm1WhbFoxo1tm1WhbFoxo1tm1Whb

absent vitelline blood vessels_Foxo1<tm1Whb>/Foxo1<tm1Whb>

表現型アノテーション

MGI marker

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

• forkhead box O1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1890077

遺伝子型

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

• Foxo1<tm1Whb>/Foxo1<tm1Whb>

アレルシンボル

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

• Foxo1<tm1Whb>

遺伝的背景

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

• Not Specified

MP annotation

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

• absent vitelline blood vessels
  http://purl.obolibrary.org/obo/MP_0001719

文献

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

• Taisuke. Hosaka, et.al., Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification., Proceedings of the National Academy of Sciences of the United States of America, 2004, 101
  http://rdf.ncbi.nlm.nih.gov/pubmed/14978268