abnormal muscle development_Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>

http://metadb.riken.jp/0000733I129S1Sv129X1SvJC57BL6Mgat2tm11JxmMgat2tm11JxmMgat2tm11Jxm

abnormal muscle development_Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>

表現型アノテーション

MGI marker

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

• mannoside acetylglucosaminyltransferase 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2384966

遺伝子型

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

• Mgat2<tm1.1Jxm>/Mgat2<tm1.1Jxm>

アレルシンボル

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

• Mgat2<tm1.1Jxm>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• abnormal muscle development
  http://purl.obolibrary.org/obo/MP_0000733

文献

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

• Y. Wang, et.al., Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis., Glycobiology, 2001, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/11805078