abnormal cardiac epithelial to mesenchymal transition_Notch1<tm2Agt>/Notch1<tm2Agt>

http://metadb.riken.jp/0008825I129SvNotch1tm2AgtNotch1tm2AgtNotch1tm2Agt

abnormal cardiac epithelial to mesenchymal transition_Notch1<tm2Agt>/Notch1<tm2Agt>

表現型アノテーション

MGI marker

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

• notch 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:97363

遺伝子型

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

• Notch1<tm2Agt>/Notch1<tm2Agt>

アレルシンボル

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

• Notch1<tm2Agt>

遺伝的背景

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

• involves: 129/Sv

MP annotation

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

• abnormal cardiac epithelial to mesenchymal transition
  http://purl.obolibrary.org/obo/MP_0008825

文献

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

• Andreas. Fischer, et.al., Combined loss of Hey1 and HeyL causes congenital heart defects because of impaired epithelial to mesenchymal transition., Circulation research, 2007, 100
  http://rdf.ncbi.nlm.nih.gov/pubmed/17303760