abnormal eye development_Msx2<tm1Rilm>/Msx2<tm1Rilm>

http://metadb.riken.jp/0001286I129S4SvJaeMsx2tm1RilmMsx2tm1RilmMsx2tm1Rilm

abnormal eye development_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

• involves: 129S4/SvJae

MP annotation

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

• abnormal eye development
  http://purl.obolibrary.org/obo/MP_0001286

文献

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

• Jiangyue. Zhao, et.al., Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly., The American journal of pathology, 2012, 180
  http://rdf.ncbi.nlm.nih.gov/pubmed/22503753