abnormal QRS complex_Ts(17<16>)65Dn/0

http://metadb.riken.jp/0003898IC3HHeHC3HHeSnC57BL6EiC57BL6JDBA2JTs171665Dn0Ts171665Dn

abnormal QRS complex_Ts(17<16>)65Dn/0

表現型アノテーション

MGI marker

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

• 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

• Ts(17<16>)65Dn/0

アレルシンボル

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

• Ts(17<16>)65Dn

遺伝的背景

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

• involves: C3H/HeH * C3H/HeSn * C57BL/6Ei * C57BL/6J * DBA/2J

MP annotation

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

• abnormal QRS complex
  http://purl.obolibrary.org/obo/MP_0003898

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