omphalocele_Psen1<tm1Bdes>/Psen1<tm1Bdes>

http://metadb.riken.jp/0003052I129P2OlaHsdPsen1tm1BdesPsen1tm1BdesPsen1tm1Bdes

omphalocele_Psen1<tm1Bdes>/Psen1<tm1Bdes>

表現型アノテーション

MGI marker

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

• presenilin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1202717

遺伝子型

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

• Psen1<tm1Bdes>/Psen1<tm1Bdes>

アレルシンボル

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

• Psen1<tm1Bdes>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• omphalocele
  http://purl.obolibrary.org/obo/MP_0003052

文献

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

• D. Hartmann, et.al., Presenilin-1 deficiency leads to loss of Cajal-Retzius neurons and cortical dysplasia similar to human type 2 lissencephaly., Current biology : CB, 1999, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/10421573