ventricular septal defect_Tbx1<tm2.1Bem>/Tbx1<tm2.2Bem>,Foxg1<tm1(cre)Skm>/Foxg1<+>

http://metadb.riken.jp/0010402I129SvC57BL6SJLSwissWebsterTbx1tm21BemTbx1tm22BemFoxg1tm1creSkmFoxg1Foxg1tm1creSkmTbx1tm21BemTbx1tm22BemFoxg1

ventricular septal defect_Tbx1<tm2.1Bem>/Tbx1<tm2.2Bem>,Foxg1<tm1(cre)Skm>/Foxg1<+>

表現型アノテーション

MGI marker

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

• forkhead box G1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347464
• T-box 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:98493

遺伝子型

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

• Tbx1<tm2.1Bem>/Tbx1<tm2.2Bem>,Foxg1<tm1(cre)Skm>/Foxg1<+>

アレルシンボル

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

• Foxg1<tm1(cre)Skm>|Tbx1<tm2.1Bem>|Tbx1<tm2.2Bem>|Foxg1<+>

遺伝的背景

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

• involves: 129/Sv * C57BL/6 * SJL * Swiss Webster

MP annotation

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

• ventricular septal defect
  http://purl.obolibrary.org/obo/MP_0010402

文献

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

• Jelena S. Arnold, et.al., Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations., Development (Cambridge, England), 2006, 133
  http://rdf.ncbi.nlm.nih.gov/pubmed/16452092