encephalomeningocele_Cecr2<tm1.1Hemc>/Cecr2<tm1.1Hemc>

http://metadb.riken.jp/0012260IFVBNCecr2tm11HemcCecr2tm11HemcCecr2tm11Hemc

encephalomeningocele_Cecr2<tm1.1Hemc>/Cecr2<tm1.1Hemc>

表現型アノテーション

MGI marker

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

• CECR2, histone acetyl-lysine reader
  http://metadb.riken.jp/db/mgi_rdf/MGI:1923799

遺伝子型

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

• Cecr2<tm1.1Hemc>/Cecr2<tm1.1Hemc>

アレルシンボル

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

• Cecr2<tm1.1Hemc>

遺伝的背景

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

• involves: FVB/N

MP annotation

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

• encephalomeningocele
  http://purl.obolibrary.org/obo/MP_0012260

文献

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

• Nicholas A. Fairbridge, et.al., Cecr2 mutations causing exencephaly trigger misregulation of mesenchymal/ectodermal transcription factors., Birth defects research. Part A, Clinical and molecular teratology, 2010, 88
  http://rdf.ncbi.nlm.nih.gov/pubmed/20589882