abnormal copper level_Atp7b<tm1Tcg>/Atp7b<tm1Tcg>

http://metadb.riken.jp/0003952I129S1SvAtp7btm1TcgAtp7btm1TcgAtp7btm1Tcg

abnormal copper level_Atp7b<tm1Tcg>/Atp7b<tm1Tcg>

表現型アノテーション

MGI marker

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

• ATPase, Cu++ transporting, beta polypeptide
  http://metadb.riken.jp/db/mgi_rdf/MGI:103297

遺伝子型

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

• Atp7b<tm1Tcg>/Atp7b<tm1Tcg>

アレルシンボル

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

• Atp7b<tm1Tcg>

遺伝的背景

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

• involves: 129S1/Sv

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

• O I. Buiakova, et.al., Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation., Human molecular genetics, 1999, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/10441329