persistent truncus arteriosis_Mecom<tm2.2Aspe>/Mecom<tm2.2Aspe>

http://metadb.riken.jp/0002633I129C57BL6JFVBNMecomtm22AspeMecomtm22AspeMecomtm22Aspe

persistent truncus arteriosis_Mecom<tm2.2Aspe>/Mecom<tm2.2Aspe>

表現型アノテーション

MGI marker

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

• MDS1 and EVI1 complex locus
  http://metadb.riken.jp/db/mgi_rdf/MGI:95457

遺伝子型

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

• Mecom<tm2.2Aspe>/Mecom<tm2.2Aspe>

アレルシンボル

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

• Mecom<tm2.2Aspe>

遺伝的背景

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

• involves: 129 * C57BL/6J * FVB/N

MP annotation

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

• persistent truncus arteriosis
  http://purl.obolibrary.org/obo/MP_0002633

文献

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

• Emilie A. Bard-Chapeau, et.al., Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects., PloS one, 2014, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/24586749