abnormal orbit morphology_Foxc2<tm1Miu>/Foxc2<+>

http://metadb.riken.jp/0010030I129P2OlaHsdC57BL6C57BL6JFoxc2tm1MiuFoxc2Foxc2Foxc2tm1Miu

abnormal orbit morphology_Foxc2<tm1Miu>/Foxc2<+>

表現型アノテーション

MGI marker

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

• forkhead box C2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347481

遺伝子型

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

• Foxc2<tm1Miu>/Foxc2<+>

アレルシンボル

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

• Foxc2<+>|Foxc2<tm1Miu>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J

MP annotation

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

• abnormal orbit morphology
  http://purl.obolibrary.org/obo/MP_0010030

文献

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

• Benjamin M. Kriederman, et.al., FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome., Human molecular genetics, 2003, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/12719382