absent heartbeat_Slc8a1<m51207Hubr>/Slc8a1<m51207Hubr>

http://metadb.riken.jp/0004086IC57BL6FVBNSlc8a1m51207HubrSlc8a1m51207HubrSlc8a1m51207Hubr

absent heartbeat_Slc8a1<m51207Hubr>/Slc8a1<m51207Hubr>

表現型アノテーション

MGI marker

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

• solute carrier family 8 (sodium/calcium exchanger), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:107956

遺伝子型

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

• Slc8a1<m51207Hubr>/Slc8a1<m51207Hubr>

アレルシンボル

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

• Slc8a1<m51207Hubr>

遺伝的背景

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

• involves: C57BL/6 * FVB/N

MP annotation

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

• absent heartbeat
  http://purl.obolibrary.org/obo/MP_0004086

文献

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

• Carolien. Wansleeben, et.al., A novel mutant allele of Ncx1: a single amino acid substitution leads to cardiac dysfunction., The International journal of developmental biology, 2010, 54
  http://rdf.ncbi.nlm.nih.gov/pubmed/21302256