persistent truncus arteriosis_Aldh1a2<tm1Dll>/Aldh1a2<tm1Ipc>

http://metadb.riken.jp/0002633ICD1Aldh1a2tm1DllAldh1a2tm1IpcAldh1a2tm1DllAldh1a2tm1Ipc

persistent truncus arteriosis_Aldh1a2<tm1Dll>/Aldh1a2<tm1Ipc>

表現型アノテーション

MGI marker

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

• aldehyde dehydrogenase family 1, subfamily A2
  http://metadb.riken.jp/db/mgi_rdf/MGI:107928

遺伝子型

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

• Aldh1a2<tm1Dll>/Aldh1a2<tm1Ipc>

アレルシンボル

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

• Aldh1a2<tm1Dll>|Aldh1a2<tm1Ipc>

遺伝的背景

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

• involves: CD-1

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

• Julien. Vermot, et.al., Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice., Proceedings of the National Academy of Sciences of the United States of America, 2003, 100
  http://rdf.ncbi.nlm.nih.gov/pubmed/12563036