abnormal circulating amino acid level_Slc38a3<m1Ingm>/Slc38a3<m1Ingm>

http://metadb.riken.jp/0005311B6C3FeSlc38a3m1IngmSlc38a3m1IngmSlc38a3m1IngmSlc38a3m1Ingm

abnormal circulating amino acid level_Slc38a3<m1Ingm>/Slc38a3<m1Ingm>

表現型アノテーション

MGI marker

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

• solute carrier family 38, member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1923507

遺伝子型

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

• Slc38a3<m1Ingm>/Slc38a3<m1Ingm>

アレルシンボル

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

• Slc38a3<m1Ingm>

遺伝的背景

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

• B6.C3Fe-Slc38a3<m1Ingm>

MP annotation

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

• abnormal circulating amino acid level
  http://purl.obolibrary.org/obo/MP_0005311

文献

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

• Kessara. Chan, et.al., Loss of function mutation of the Slc38a3 glutamine transporter reveals its critical role for amino acid metabolism in the liver, brain, and kidney., Pflugers Archiv : European journal of physiology, 2016, 468
  http://rdf.ncbi.nlm.nih.gov/pubmed/26490457