abnormal telencephalon development_Ikbkap<tm1.1Id>/Ikbkap<tm1.1Id>

http://metadb.riken.jp/0000934I129S1SvC57BL6CBAIkbkaptm11IdIkbkaptm11IdIkbkaptm11Id

abnormal telencephalon development_Ikbkap<tm1.1Id>/Ikbkap<tm1.1Id>

表現型アノテーション

MGI marker

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

• inhibitor of kappa light polypeptide enhancer in B cells, kinase complex-associated protein
  http://metadb.riken.jp/db/mgi_rdf/MGI:1914544

遺伝子型

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

• Ikbkap<tm1.1Id>/Ikbkap<tm1.1Id>

アレルシンボル

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

• Ikbkap<tm1.1Id>

遺伝的背景

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

• involves: 129S1/Sv * C57BL/6 * CBA

MP annotation

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

• abnormal telencephalon development
  http://purl.obolibrary.org/obo/MP_0000934

文献

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

• Paula. Dietrich, et.al., Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality., PloS one, 2011, 6
  http://rdf.ncbi.nlm.nih.gov/pubmed/22046433