abnormal heart electrocardiography waveform feature_Del(16App-Runx1)5Yah/Ts(17<16>)65Dn

http://metadb.riken.jp/0010508IBALBcC3HC57BL6DBA2JDel16AppRunx15YahTs171665DnDel16AppRunx15YahTs171665Dn

abnormal heart electrocardiography waveform feature_Del(16App-Runx1)5Yah/Ts(17<16>)65Dn

表現型アノテーション

MGI marker

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

• deletion, Chr 16, Yann Herault 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:5431226
• trisomy, Chr 16 translocation to Chr 17, Davisson 65
  http://metadb.riken.jp/db/mgi_rdf/MGI:2178111

遺伝子型

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

• Del(16App-Runx1)5Yah/Ts(17<16>)65Dn

アレルシンボル

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

• Del(16App-Runx1)5Yah|Ts(17<16>)65Dn

遺伝的背景

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

• involves: BALB/c * C3H * C57BL/6 * DBA/2J

MP annotation

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

• abnormal heart electrocardiography waveform feature
  http://purl.obolibrary.org/obo/MP_0010508

文献

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

• Matthieu. Raveau, et.al., The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse model., PLoS genetics, 2012, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/22693452