abnormal craniofacial development_Nfib<tm1Rmg>/Nfib<tm1Rmg>

http://metadb.riken.jp/0003935I129P2OlaHsdC57BL6Nfibtm1RmgNfibtm1RmgNfibtm1Rmg

abnormal craniofacial development_Nfib<tm1Rmg>/Nfib<tm1Rmg>

表現型アノテーション

MGI marker

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

• nuclear factor I/B
  http://metadb.riken.jp/db/mgi_rdf/MGI:103188

遺伝子型

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

• Nfib<tm1Rmg>/Nfib<tm1Rmg>

アレルシンボル

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

• Nfib<tm1Rmg>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal craniofacial development
  http://purl.obolibrary.org/obo/MP_0003935

文献

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

• Lisenka E L M. Vissers, et.al., Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice., PLoS genetics, 2011, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/21931569