no abnormal phenotype detected_Pmm2<tm1.1Cknr>/Pmm2<tm1.1Cknr>

http://metadb.riken.jp/0002169IC57BL6JPmm2tm11CknrPmm2tm11CknrPmm2tm11Cknr

no abnormal phenotype detected_Pmm2<tm1.1Cknr>/Pmm2<tm1.1Cknr>

表現型アノテーション

MGI marker

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

• phosphomannomutase 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1859214

遺伝子型

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

• Pmm2<tm1.1Cknr>/Pmm2<tm1.1Cknr>

アレルシンボル

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

• Pmm2<tm1.1Cknr>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Anette. Schneider, et.al., Successful prenatal mannose treatment for congenital disorder of glycosylation-Ia in mice., Nature medicine, 2011, 18
  http://rdf.ncbi.nlm.nih.gov/pubmed/22157680