nephrocalcinosis_Agxt<tm1Ull>/Agxt<tm1Ull>

http://metadb.riken.jp/0003197B6129X1Agxttm1UllAgxttm1UllAgxttm1UllAgxttm1Ull

nephrocalcinosis_Agxt<tm1Ull>/Agxt<tm1Ull>

表現型アノテーション

MGI marker

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

• alanine-glyoxylate aminotransferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1329033

遺伝子型

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

• Agxt<tm1Ull>/Agxt<tm1Ull>

アレルシンボル

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

• Agxt<tm1Ull>

遺伝的背景

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

• B6.129X1-Agxt<tm1Ull>

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

• Eduardo C. Salido, et.al., Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer., Proceedings of the National Academy of Sciences of the United States of America, 2006, 103
  http://rdf.ncbi.nlm.nih.gov/pubmed/17110443