no abnormal phenotype detected_Pkhd1<tm1Ggg>/Pkhd1<tm1Ggg>

http://metadb.riken.jp/0002169I129SSvEvC57BL6Pkhd1tm1GggPkhd1tm1GggPkhd1tm1Ggg

no abnormal phenotype detected_Pkhd1<tm1Ggg>/Pkhd1<tm1Ggg>

表現型アノテーション

MGI marker

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

• polycystic kidney and hepatic disease 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2155808

遺伝子型

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

• Pkhd1<tm1Ggg>/Pkhd1<tm1Ggg>

アレルシンボル

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

• Pkhd1<tm1Ggg>

遺伝的背景

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

• involves: 129S/SvEv * 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

• Miguel A. Garcia-Gonzalez, et.al., Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway., Human molecular genetics, 2007, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/17575307