dystrophic muscle_Pomgnt1<Gt(OST179231)Lex>/Pomgnt1<Gt(OST179231)Lex>

http://metadb.riken.jp/0000752I129S5SvEvBrdC57BL6JPomgnt1GtOST179231LexPomgnt1GtOST179231LexPomgnt1GtOST179231Lex

dystrophic muscle_Pomgnt1<Gt(OST179231)Lex>/Pomgnt1<Gt(OST179231)Lex>

表現型アノテーション

MGI marker

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

• protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1915523

遺伝子型

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

• Pomgnt1<Gt(OST179231)Lex>/Pomgnt1<Gt(OST179231)Lex>

アレルシンボル

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

• Pomgnt1<Gt(OST179231)Lex>

遺伝的背景

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

• involves: 129S5/SvEvBrd * C57BL/6J

MP annotation

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

• dystrophic muscle
  http://purl.obolibrary.org/obo/MP_0000752

文献

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

• Jianmin. Liu, et.al., A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)., Mechanisms of development, 2006, 123
  http://rdf.ncbi.nlm.nih.gov/pubmed/16458488