no abnormal phenotype detected_Pkd1<tm1.1Djmp>/Pkd1<tm1.1Djmp>

http://metadb.riken.jp/0002169I129P2OlaHsdC57BL6Pkd1tm11DjmpPkd1tm11DjmpPkd1tm11Djmp

no abnormal phenotype detected_Pkd1<tm1.1Djmp>/Pkd1<tm1.1Djmp>

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<tm1.1Djmp>/Pkd1<tm1.1Djmp>

アレルシンボル

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

• Pkd1<tm1.1Djmp>

遺伝的背景

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

• involves: 129P2/OlaHsd * 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

• Irma S. Lantinga-van Leeuwen, et.al., Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease., Human molecular genetics, 2004, 13
  http://rdf.ncbi.nlm.nih.gov/pubmed/15496422