persistent truncus arteriosis_Chrd<tm1Emdr>/Chrd<tm1Emdr>,Tbx1<m1Jlk>/Tbx1<m1Jlk>

http://metadb.riken.jp/0002633129SvTbx1m1JlkChrdtm1EmdrChrdtm1EmdrChrdtm1EmdrTbx1m1JlkTbx1m1JlkChrdtm1EmdrTbx1m1Jlk

persistent truncus arteriosis_Chrd<tm1Emdr>/Chrd<tm1Emdr>,Tbx1<m1Jlk>/Tbx1<m1Jlk>

表現型アノテーション

MGI marker

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

• T-box 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:98493
• chordin
  http://metadb.riken.jp/db/mgi_rdf/MGI:1313268

遺伝子型

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

• Chrd<tm1Emdr>/Chrd<tm1Emdr>,Tbx1<m1Jlk>/Tbx1<m1Jlk>

アレルシンボル

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

• Chrd<tm1Emdr>|Tbx1<m1Jlk>

遺伝的背景

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

• 129/Sv-Tbx1<m1Jlk> Chrd<tm1Emdr>

MP annotation

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

• persistent truncus arteriosis
  http://purl.obolibrary.org/obo/MP_0002633

文献

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

• Murim. Choi, et.al., Chordin is a modifier of tbx1 for the craniofacial malformations of 22q11 deletion syndrome phenotypes in mouse., PLoS genetics, 2009, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/19247433