abnormal somite development_Pofut1<cax>/Pofut1<cax>

http://metadb.riken.jp/0001688C3HHeJPofut1caxJPofut1caxPofut1caxPofut1cax

abnormal somite development_Pofut1<cax>/Pofut1<cax>

表現型アノテーション

MGI marker

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

• protein O-fucosyltransferase 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153207

遺伝子型

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

• Pofut1<cax>/Pofut1<cax>

アレルシンボル

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

• Pofut1<cax>

遺伝的背景

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

• C3H/HeJ-Pofut1<cax>/J

MP annotation

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

• abnormal somite development
  http://purl.obolibrary.org/obo/MP_0001688

文献

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

• Karin. Schuster-Gossler, et.al., Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development., BMC developmental biology, 2009, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/19161597