abnormal skeleton development_Pkd1<tm1Hung>/Pkd1<tm1Hung>

http://metadb.riken.jp/0002113EI129P2OlaHsdC57BL6orI129P2OlaHsdFVBPkd1tm1HungPkd1tm1HungPkd1tm1Hung

abnormal skeleton development_Pkd1<tm1Hung>/Pkd1<tm1Hung>

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<tm1Hung>/Pkd1<tm1Hung>

アレルシンボル

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

• Pkd1<tm1Hung>

遺伝的背景

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

• either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• abnormal skeleton development
  http://purl.obolibrary.org/obo/MP_0002113

文献

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

• Si-Tse. Jiang, et.al., Defining a link with autosomal-dominant polycystic kidney disease in mice with congenitally low expression of Pkd1., The American journal of pathology, 2006, 168
  http://rdf.ncbi.nlm.nih.gov/pubmed/16400024