abnormal axon morphology_Efnb2<tm1Henk>/Efnb2<tm1Henk>,Efnb2<tm3.1Henk>/Efnb2<tm3.1Henk>

http://metadb.riken.jp/0005404I129S1Sv129X1SvJEfnb2tm1HenkEfnb2tm1HenkEfnb2tm31HenkEfnb2tm31HenkEfnb2tm31HenkEfnb2tm1Henk

abnormal axon morphology_Efnb2<tm1Henk>/Efnb2<tm1Henk>,Efnb2<tm3.1Henk>/Efnb2<tm3.1Henk>

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<tm1Henk>/Efnb2<tm1Henk>,Efnb2<tm3.1Henk>/Efnb2<tm3.1Henk>

アレルシンボル

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

• Efnb2<tm3.1Henk>|Efnb2<tm1Henk>

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 axon morphology
  http://purl.obolibrary.org/obo/MP_0005404

文献

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

• Sonal. Thakar, et.al., Critical roles for EphB and ephrin-B bidirectional signalling in retinocollicular mapping., Nature communications, 2011, 2
  http://rdf.ncbi.nlm.nih.gov/pubmed/21847105