abnormal copper level_Slc31a1<tm1Djt>/Slc31a1<+>

http://metadb.riken.jp/0003952I129S1Sv129X1SvJC57BL6Slc31a1tm1DjtSlc31a1Slc31a1Slc31a1tm1Djt

abnormal copper level_Slc31a1<tm1Djt>/Slc31a1<+>

表現型アノテーション

MGI marker

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

• solute carrier family 31, member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1333843

遺伝子型

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

• Slc31a1<tm1Djt>/Slc31a1<+>

アレルシンボル

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

• Slc31a1<+>|Slc31a1<tm1Djt>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• abnormal copper level
  http://purl.obolibrary.org/obo/MP_0003952

文献

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

• J. Lee, et.al., Essential role for mammalian copper transporter Ctr1 in copper homeostasis and embryonic development., Proceedings of the National Academy of Sciences of the United States of America, 2001, 98
  http://rdf.ncbi.nlm.nih.gov/pubmed/11391005