abnormal axial skeleton morphology_Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>

http://metadb.riken.jp/0002114I129S1SvImJC57BL6JLfngtm1GridLfngtm1GridRfngtm1GridRfngtm1GridRfngtm1GridLfngtm1Grid

abnormal axial skeleton morphology_Lfng<tm1Grid>/Lfng<tm1Grid>,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
• LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1095413

遺伝子型

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

• Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>

アレルシンボル

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

• Rfng<tm1Grid>|Lfng<tm1Grid>

遺伝的背景

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

• involves: 129S1/SvImJ * C57BL/6J

MP annotation

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

• abnormal axial skeleton morphology
  http://purl.obolibrary.org/obo/MP_0002114

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