microphthalmia_Slc40a1<ffe>/Slc40a1<ffe>

http://metadb.riken.jp/0001297IC3HHeJC57BL6JSlc40a1ffeSlc40a1ffeSlc40a1ffe

microphthalmia_Slc40a1<ffe>/Slc40a1<ffe>

表現型アノテーション

MGI marker

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

• solute carrier family 40 (iron-regulated transporter), member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1315204

遺伝子型

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

• Slc40a1<ffe>/Slc40a1<ffe>

アレルシンボル

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

• Slc40a1<ffe>

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6J

MP annotation

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

• microphthalmia
  http://purl.obolibrary.org/obo/MP_0001297

文献

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

• Irene E. Zohn, et.al., The flatiron mutation in mouse ferroportin acts as a dominant negative to cause ferroportin disease., Blood, 2007, 109
  http://rdf.ncbi.nlm.nih.gov/pubmed/17289807