abnormal retinal development_Vsx2<tm1.1Eml>/Vsx2<tm1.1Eml>

http://metadb.riken.jp/0009772I129S1Sv129X1SvJVsx2tm11EmlVsx2tm11EmlVsx2tm11Eml

abnormal retinal development_Vsx2<tm1.1Eml>/Vsx2<tm1.1Eml>

表現型アノテーション

MGI marker

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

• visual system homeobox 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:88401

遺伝子型

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

• Vsx2<tm1.1Eml>/Vsx2<tm1.1Eml>

アレルシンボル

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

• Vsx2<tm1.1Eml>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ

MP annotation

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

• abnormal retinal development
  http://purl.obolibrary.org/obo/MP_0009772

文献

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

• Changjiang. Zou, et.al., Vsx2 controls eye organogenesis and retinal progenitor identity via homeodomain and non-homeodomain residues required for high affinity DNA binding., PLoS genetics, 2012, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/23028343