absent corpus callosum_Nfia<tm1Rmg>/Nfia<tm1Rmg>

http://metadb.riken.jp/0002196I129P2OlaHsdBlackSwissNfiatm1RmgNfiatm1RmgNfiatm1Rmg

absent corpus callosum_Nfia<tm1Rmg>/Nfia<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/A
  http://metadb.riken.jp/db/mgi_rdf/MGI:108056

遺伝子型

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

• Nfia<tm1Rmg>/Nfia<tm1Rmg>

アレルシンボル

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

• Nfia<tm1Rmg>

遺伝的背景

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

• involves: 129P2/OlaHsd * Black Swiss

MP annotation

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

• absent corpus callosum
  http://purl.obolibrary.org/obo/MP_0002196

文献

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

• L. das Neves, et.al., Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum., Proceedings of the National Academy of Sciences of the United States of America, 1999, 96
  http://rdf.ncbi.nlm.nih.gov/pubmed/10518556