hemopericardium_Runx1<tm7Spe>/Runx1<tm7Spe>

http://metadb.riken.jp/0005244I129SvC57BL6Runx1tm7SpeRunx1tm7SpeRunx1tm7Spe

hemopericardium_Runx1<tm7Spe>/Runx1<tm7Spe>

表現型アノテーション

MGI marker

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

• runt related transcription factor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:99852

遺伝子型

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

• Runx1<tm7Spe>/Runx1<tm7Spe>

アレルシンボル

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

• Runx1<tm7Spe>

遺伝的背景

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

• involves: 129/Sv * C57BL/6

MP annotation

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

• hemopericardium
  http://purl.obolibrary.org/obo/MP_0005244

文献

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

• Christina J. Matheny, et.al., Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles., The EMBO journal, 2007, 26
  http://rdf.ncbi.nlm.nih.gov/pubmed/17290219