no abnormal phenotype detected_Ufd1<tm1Bld>/Ufd1<+>

http://metadb.riken.jp/0002169I129S7SvEvBrdC57BL6Ufd1tm1BldUfd1Ufd1Ufd1tm1Bld

no abnormal phenotype detected_Ufd1<tm1Bld>/Ufd1<+>

表現型アノテーション

MGI marker

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

• ubiquitin recognition factor in ER-associated degradation 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:109353

遺伝子型

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

• Ufd1<tm1Bld>/Ufd1<+>

アレルシンボル

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

• Ufd1<+>|Ufd1<tm1Bld>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

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

• E A. Lindsay, et.al., Congenital heart disease in mice deficient for the DiGeorge syndrome region., Nature, 1999, 401
  http://rdf.ncbi.nlm.nih.gov/pubmed/10517636