abnormal erythropoiesis_Lhx2<tm1Dra>/Lhx2<tm1Dra>

http://metadb.riken.jp/0000245I129S4SvJaeLhx2tm1DraLhx2tm1DraLhx2tm1Dra

abnormal erythropoiesis_Lhx2<tm1Dra>/Lhx2<tm1Dra>

表現型アノテーション

MGI marker

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

• LIM homeobox protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:96785

遺伝子型

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

• Lhx2<tm1Dra>/Lhx2<tm1Dra>

アレルシンボル

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

• Lhx2<tm1Dra>

遺伝的背景

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

• involves: 129S4/SvJae

MP annotation

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

• abnormal erythropoiesis
  http://purl.obolibrary.org/obo/MP_0000245

文献

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

• 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