no abnormal phenotype detected_Pkd1<tm2.1Bol>/Pkd1<tm2.2Bol>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6C57BL6NTacPkd1tm21BolPkd1tm22BolPkd1tm21BolPkd1tm22Bol

no abnormal phenotype detected_Pkd1<tm2.1Bol>/Pkd1<tm2.2Bol>

表現型アノテーション

MGI marker

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

• polycystic kidney disease 1 homolog
  http://metadb.riken.jp/db/mgi_rdf/MGI:97603

遺伝子型

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

• Pkd1<tm2.1Bol>/Pkd1<tm2.2Bol>

アレルシンボル

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

• Pkd1<tm2.1Bol>|Pkd1<tm2.2Bol>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6 * C57BL/6NTac

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

• Claas. Wodarczyk, et.al., A novel mouse model reveals that polycystin-1 deficiency in ependyma and choroid plexus results in dysfunctional cilia and hydrocephalus., PloS one, 2009, 4
  http://rdf.ncbi.nlm.nih.gov/pubmed/19774080