anemia_Unc13d<Jinx>/Unc13d<Jinx>

http://metadb.riken.jp/0001577C57BL6JUnc13dJinxMmucdUnc13dJinxUnc13dJinxUnc13dJinx

anemia_Unc13d<Jinx>/Unc13d<Jinx>

表現型アノテーション

MGI marker

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

• unc-13 homolog D (C. elegans)
  http://metadb.riken.jp/db/mgi_rdf/MGI:1917700

遺伝子型

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

• Unc13d<Jinx>/Unc13d<Jinx>

アレルシンボル

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

• Unc13d<Jinx>

遺伝的背景

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

• C57BL/6J-Unc13d<Jinx>/Mmucd

MP annotation

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

• anemia
  http://purl.obolibrary.org/obo/MP_0001577

文献

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

• Karine. Crozat, et.al., Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis., The Journal of experimental medicine, 2007, 204
  http://rdf.ncbi.nlm.nih.gov/pubmed/17420270