complete atrioventricular septal defect_Megf8<hlb611>/Megf8<hlb611>

http://metadb.riken.jp/0010413IC57BL6JC3HHeJMegf8hlb611Megf8hlb611Megf8hlb611

complete atrioventricular septal defect_Megf8<hlb611>/Megf8<hlb611>

表現型アノテーション

MGI marker

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

• multiple EGF-like-domains 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:2446294

遺伝子型

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

• Megf8<hlb611>/Megf8<hlb611>

アレルシンボル

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

• Megf8<hlb611>

遺伝的背景

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

• involves: C57BL/6J * C3H/HeJ

MP annotation

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

• complete atrioventricular septal defect
  http://purl.obolibrary.org/obo/MP_0010413

文献

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

• Christine N. Aune, et.al., Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies., Pediatric research, 2008, 63
  http://rdf.ncbi.nlm.nih.gov/pubmed/18043505