abnormal cardiac epithelial to mesenchymal transition_Hey2<tm1Gess>/Hey2<tm1Gess>

http://metadb.riken.jp/0008825I129P2OlaHsdHey2tm1GessHey2tm1GessHey2tm1Gess

abnormal cardiac epithelial to mesenchymal transition_Hey2<tm1Gess>/Hey2<tm1Gess>

表現型アノテーション

MGI marker

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

• hairy/enhancer-of-split related with YRPW motif 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1341884

遺伝子型

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

• Hey2<tm1Gess>/Hey2<tm1Gess>

アレルシンボル

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

• Hey2<tm1Gess>

遺伝的背景

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

• involves: 129P2/OlaHsd

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