no abnormal phenotype detected_Efnb2<tm2.1Kln>/Efnb2<tm2.1Kln>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJC57BL6Efnb2tm21KlnEfnb2tm21KlnEfnb2tm21Kln

no abnormal phenotype detected_Efnb2<tm2.1Kln>/Efnb2<tm2.1Kln>

表現型アノテーション

MGI marker

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

• ephrin B2
  http://metadb.riken.jp/db/mgi_rdf/MGI:105097

遺伝子型

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

• Efnb2<tm2.1Kln>/Efnb2<tm2.1Kln>

アレルシンボル

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

• Efnb2<tm2.1Kln>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• R H. Adams, et.al., The cytoplasmic domain of the ligand ephrinB2 is required for vascular morphogenesis but not cranial neural crest migration., Cell, 2001, 104
  http://rdf.ncbi.nlm.nih.gov/pubmed/11163240