absent cerebellum vermis lobule IX_Msx2<tm1Rilm>/Msx2<tm1Rilm>

http://metadb.riken.jp/0000871EI129S4SvJaeorI129S4SvJaeBALBcorI129S4SvJaeC57BL6JMsx2tm1RilmMsx2tm1RilmMsx2tm1Rilm

absent cerebellum vermis lobule IX_Msx2<tm1Rilm>/Msx2<tm1Rilm>

表現型アノテーション

MGI marker

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

• msh homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97169

遺伝子型

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

• Msx2<tm1Rilm>/Msx2<tm1Rilm>

アレルシンボル

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

• Msx2<tm1Rilm>

遺伝的背景

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

• either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)

MP annotation

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

• absent cerebellum vermis lobule IX
  http://purl.obolibrary.org/obo/MP_0000871

文献

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

• I. Satokata, et.al., Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation., Nature genetics, 2000, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/10742104