no abnormal phenotype detected_Cul4b<tm1Yxg>/Y

http://metadb.riken.jp/0002169I129X1SvJCul4btm1YxgYCul4btm1Yxg

no abnormal phenotype detected_Cul4b<tm1Yxg>/Y

表現型アノテーション

MGI marker

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

• cullin 4B
  http://metadb.riken.jp/db/mgi_rdf/MGI:1919834

遺伝子型

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

• Cul4b<tm1Yxg>/Y

アレルシンボル

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

• Cul4b<tm1Yxg>

遺伝的背景

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

• involves: 129X1/SvJ

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

• Baichun. Jiang, et.al., Lack of Cul4b, an E3 ubiquitin ligase component, leads to embryonic lethality and abnormal placental development., PloS one, 2012, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/22606329