inlet ventricular septal defect_Del(11Mpo-Chad)18Brd/+

http://metadb.riken.jp/0010419I129S7SvEvBrdC57BL6Del11MpoChad18BrdDel11MpoChad18Brd

inlet ventricular septal defect_Del(11Mpo-Chad)18Brd/+

表現型アノテーション

MGI marker

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

• deletion, Chr 11, Bradley 18
  http://metadb.riken.jp/db/mgi_rdf/MGI:3653212

遺伝子型

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

• Del(11Mpo-Chad)18Brd/+

アレルシンボル

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

• Del(11Mpo-Chad)18Brd|+

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

MP annotation

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

• inlet ventricular septal defect
  http://purl.obolibrary.org/obo/MP_0010419

文献

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

• Y Eugene. Yu, et.al., A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice., Genetics, 2006, 173
  http://rdf.ncbi.nlm.nih.gov/pubmed/16489219