no abnormal phenotype detected_Pkd1l1<rks>/Pkd1l1<+>,Pkd2<lrm4>/Pkd2<+>

http://metadb.riken.jp/0002169C3CgPkd2lrm4Pkd1l1rksPkd1l1rksPkd1l1Pkd2lrm4Pkd2Pkd2lrm4Pkd1l1rksPkd1l1Pkd2

no abnormal phenotype detected_Pkd1l1<rks>/Pkd1l1<+>,Pkd2<lrm4>/Pkd2<+>

表現型アノテーション

MGI marker

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

• polycystic kidney disease 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1099818
• polycystic kidney disease 1 like 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2156538

遺伝子型

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

• Pkd1l1<rks>/Pkd1l1<+>,Pkd2<lrm4>/Pkd2<+>

アレルシンボル

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

• Pkd2<lrm4>|Pkd1l1<rks>|Pkd1l1<+>|Pkd2<+>

遺伝的背景

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

• C3.Cg-Pkd2<lrm4> Pkd1l1<rks>

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

• Sarah. Field, et.al., Pkd1l1 establishes left-right asymmetry and physically interacts with Pkd2., Development (Cambridge, England), 2011, 138
  http://rdf.ncbi.nlm.nih.gov/pubmed/21307093