no abnormal phenotype detected_Rfng<tm1Grid>/Rfng<tm1Grid>

http://metadb.riken.jp/0002169I129S1SvC57BL6JRfngtm1GridRfngtm1GridRfngtm1Grid

no abnormal phenotype detected_Rfng<tm1Grid>/Rfng<tm1Grid>

表現型アノテーション

MGI marker

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

• RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:894275

遺伝子型

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

• Rfng<tm1Grid>/Rfng<tm1Grid>

アレルシンボル

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

• Rfng<tm1Grid>

遺伝的背景

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

• involves: 129S1/Sv * 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

• Nian. Zhang, et.al., Segmentation defects of Notch pathway mutants and absence of a synergistic phenotype in lunatic fringe/radical fringe double mutant mice., Genesis (New York, N.Y. : 2000), 2002, 33
  http://rdf.ncbi.nlm.nih.gov/pubmed/12001066