abnormal erythropoiesis_Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>

http://metadb.riken.jp/0000245I129X1SvJSlc19a2tm1GelbSlc19a2tm1GelbSlc19a2tm1Gelb

abnormal erythropoiesis_Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>

表現型アノテーション

MGI marker

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

• solute carrier family 19 (thiamine transporter), member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1928761

遺伝子型

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

• Slc19a2<tm1Gelb>/Slc19a2<tm1Gelb>

アレルシンボル

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

• Slc19a2<tm1Gelb>

遺伝的背景

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

• involves: 129X1/SvJ

MP annotation

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

• abnormal erythropoiesis
  http://purl.obolibrary.org/obo/MP_0000245

文献

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

• Kimihiko. Oishi, et.al., Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/12393806