F D. Porter, et.al., Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development., Development (Cambridge, England), 1997, 124

http://rdf.ncbi.nlm.nih.gov/pubmed/9247336

F D. Porter, et.al., Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development., Development (Cambridge, England), 1997, 124

pubmed

allele

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

• Lhx2<tm1Dra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1890208

表現型アノテーション

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

• abnormal neocortex morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0008547I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• pallor_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0003717I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal eye development_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0001286I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• lethality throughout fetal growth and development, complete penetrance_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0011099I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal telencephalon morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000787I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• decreased erythroid progenitor cell number_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0008973I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal optic vesicle formation_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0003425I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal erythropoiesis_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000245I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• decreased hematocrit_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000208I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal head morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000432I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal cerebral cortex morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000788I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• hydrops fetalis_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0002192I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• anemia_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0001577I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• liver hypoplasia_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000600I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal basal ganglion morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0006007I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• absent retina_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0009773I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• aphakia_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0003078I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• absent hippocampus_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000809I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• anophthalmia_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0001293I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• abnormal cortical plate morphology_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0008439I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• absent optic placodes_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0012170I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• small liver_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000601I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra
• forebrain hypoplasia_Lhx2<tm1Dra>/Lhx2<tm1Dra>
  http://metadb.riken.jp/0000784I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra

class

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

• Lhx2<tm1Dra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1890208