absent coat pigmentation_Atp7a<Mo-2Btlr>/Y

http://metadb.riken.jp/0005171C57BL6JAtp7aMo2BtlrAtp7aMo2BtlrYAtp7aMo2Btlr

absent coat pigmentation_Atp7a<Mo-2Btlr>/Y

表現型アノテーション

MGI marker

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

• ATPase, Cu++ transporting, alpha polypeptide
  http://metadb.riken.jp/db/mgi_rdf/MGI:99400

遺伝子型

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

• Atp7a<Mo-2Btlr>/Y

アレルシンボル

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

• Atp7a<Mo-2Btlr>

遺伝的背景

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

• C57BL/6J-Atp7a<Mo-2Btlr>

MP annotation

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

• absent coat pigmentation
  http://purl.obolibrary.org/obo/MP_0005171

文献

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

• Owen M. Siggs, et.al., Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease., Proceedings of the National Academy of Sciences of the United States of America, 2012, 109
  http://rdf.ncbi.nlm.nih.gov/pubmed/22869751