malocclusion_Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>

http://metadb.riken.jp/0000120I129S6SvEvTacFVBNNIHBlackSwissSirt6tm22CxdSirt6tm22CxdSirt6tm22Cxd

malocclusion_Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>

表現型アノテーション

MGI marker

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

• sirtuin 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:1354161

遺伝子型

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

• Sirt6<tm2.2Cxd>/Sirt6<tm2.2Cxd>

アレルシンボル

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

• Sirt6<tm2.2Cxd>

遺伝的背景

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

• involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss

MP annotation

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

• malocclusion
  http://purl.obolibrary.org/obo/MP_0000120

文献

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

• Cuiying. Xiao, et.al., SIRT6 deficiency results in severe hypoglycemia by enhancing both basal and insulin-stimulated glucose uptake in mice., The Journal of biological chemistry, 2010, 285
  http://rdf.ncbi.nlm.nih.gov/pubmed/20847051