no abnormal phenotype detected_Cdc42<tm1.1Rac>/Cdc42<tm1.1Rac>

http://metadb.riken.jp/0002169I129P2OlaHsdFVBNCdc42tm11RacCdc42tm11RacCdc42tm11Rac

no abnormal phenotype detected_Cdc42<tm1.1Rac>/Cdc42<tm1.1Rac>

表現型アノテーション

MGI marker

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

• cell division cycle 42
  http://metadb.riken.jp/db/mgi_rdf/MGI:106211

遺伝子型

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

• Cdc42<tm1.1Rac>/Cdc42<tm1.1Rac>

アレルシンボル

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

• Cdc42<tm1.1Rac>

遺伝的背景

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

• involves: 129P2/OlaHsd * FVB/N

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

• Xu. Peng, et.al., Inactivation of Cdc42 in embryonic brain results in hydrocephalus with ependymal cell defects in mice., Protein & cell, 2013, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/23150167