no abnormal phenotype detected_Robo2<tm1Rilm>/Robo2<tm1Rilm>

http://metadb.riken.jp/0002169I129C57BL6Robo2tm1RilmRobo2tm1RilmRobo2tm1Rilm

no abnormal phenotype detected_Robo2<tm1Rilm>/Robo2<tm1Rilm>

表現型アノテーション

MGI marker

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

• roundabout guidance receptor 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1890110

遺伝子型

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

• Robo2<tm1Rilm>/Robo2<tm1Rilm>

アレルシンボル

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

• Robo2<tm1Rilm>

遺伝的背景

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

• involves: 129 * 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

• Weining. Lu, et.al., Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux., American journal of human genetics, 2007, 80
  http://rdf.ncbi.nlm.nih.gov/pubmed/17357069