abnormal kidney corticomedullary boundary morphology_Krd/Krd<+>

http://metadb.riken.jp/0011376IC3HHeC57BL6YBRKiKrdKrdKrdKrd

abnormal kidney corticomedullary boundary morphology_Krd/Krd<+>

表現型アノテーション

MGI marker

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

• kidney and retinal defects
  http://metadb.riken.jp/db/mgi_rdf/MGI:99258

遺伝子型

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

• Krd/Krd<+>

アレルシンボル

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

• Krd<+>|Krd

遺伝的背景

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

• involves: C3H/He * C57BL/6 * YBR/Ki

MP annotation

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

• abnormal kidney corticomedullary boundary morphology
  http://purl.obolibrary.org/obo/MP_0011376

文献

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

• S A. Keller, et.al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus., Genomics, 1994, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/7835879