nephrocalcinosis_Slc12a1<urehr3>/Slc12a1<urehr3>

http://metadb.riken.jp/0003197IC3HeBFeJSlc12a1urehr3Slc12a1urehr3Slc12a1urehr3

nephrocalcinosis_Slc12a1<urehr3>/Slc12a1<urehr3>

表現型アノテーション

MGI marker

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

• solute carrier family 12, member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:103150

遺伝子型

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

• Slc12a1<urehr3>/Slc12a1<urehr3>

アレルシンボル

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

• Slc12a1<urehr3>

遺伝的背景

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

• involves: C3HeB/FeJ

MP annotation

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

• nephrocalcinosis
  http://purl.obolibrary.org/obo/MP_0003197

文献

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

• Elisabeth. Kemter, et.al., Mutation of the Na(+)-K(+)-2Cl(-) cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia., American journal of physiology. Renal physiology, 2010, 298
  http://rdf.ncbi.nlm.nih.gov/pubmed/20219826