G E. Winnier, et.al., The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo., Genes & development, 1997, 11

http://rdf.ncbi.nlm.nih.gov/pubmed/9106663

G E. Winnier, et.al., The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo., Genes & development, 1997, 11

pubmed

allele

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

• Foxc2<tm1Blh>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1857865

class

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

• Foxc2<tm1Blh>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1857865

表現型アノテーション

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

• absent presphenoid bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004449I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• kinked neural tube_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0003400I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• cleft palate_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0000111I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• small exoccipital bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004445I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal vertebral arch morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004599I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• absent supraoccipital bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004443I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• small interparietal bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004384I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• absent incus_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004318I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• small basisphenoid bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004462I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal Meckel's cartilage morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0005587I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• absent palatine bone_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004476I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal squamosal bone morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004423I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• rib fusion_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0000154I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• small mandible_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004592I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• decreased rib number_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0003345I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal craniofacial bone morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0002116I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• intracranial hemorrhage_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0001915I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• embryonic lethality during organogenesis, incomplete penetrance_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0011108I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal multipotent stem cell morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0002400I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal somite shape_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0001691I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal gonial bone morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0008380I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• decreased tympanic ring size_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0006020I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal malleus morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0000029I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal blood vessel morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0001614I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal vertebral body morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0000141I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal middle ear ossicle morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0005105I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• absent stapes_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0004204I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh
• abnormal cartilage morphology_Foxc2<tm1Blh>/Foxc2<tm1Blh>
  http://metadb.riken.jp/0000163I129S6SvEvTacBlackSwissFoxc2tm1BlhFoxc2tm1BlhFoxc2tm1Blh