abnormal survival_Xpnpep1<Gt(S22-1B1)Sor>/Xpnpep1<Gt(S22-1B1)Sor>

http://metadb.riken.jp/0010769I129S4SvJaeC57BL6JXpnpep1GtS221B1SorXpnpep1GtS221B1SorXpnpep1GtS221B1Sor

abnormal survival_Xpnpep1<Gt(S22-1B1)Sor>/Xpnpep1<Gt(S22-1B1)Sor>

表現型アノテーション

MGI marker

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

• X-prolyl aminopeptidase (aminopeptidase P) 1, soluble
  http://metadb.riken.jp/db/mgi_rdf/MGI:2180003

遺伝子型

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

• Xpnpep1<Gt(S22-1B1)Sor>/Xpnpep1<Gt(S22-1B1)Sor>

アレルシンボル

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

• Xpnpep1<Gt(S22-1B1)Sor>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6J

MP annotation

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

• abnormal survival
  http://purl.obolibrary.org/obo/MP_0010769

文献

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

• Sang Ho. Yoon, et.al., Developmental retardation, microcephaly, and peptiduria in mice without aminopeptidase P1., Biochemical and biophysical research communications, 2012, 429
  http://rdf.ncbi.nlm.nih.gov/pubmed/23131567