hypoxia_Ndn<tm2Stw>/Ndn<+>

http://metadb.riken.jp/0005039I129S1SvC57BL6JNdntm2StwNdnNdntm2StwNdn

hypoxia_Ndn<tm2Stw>/Ndn<+>

表現型アノテーション

MGI marker

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

• necdin
  http://metadb.riken.jp/db/mgi_rdf/MGI:97290

遺伝子型

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

• Ndn<tm2Stw>/Ndn<+>

アレルシンボル

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

• Ndn<tm2Stw>|Ndn<+>

遺伝的背景

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

• involves: 129S1/Sv * C57BL/6J

MP annotation

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

• hypoxia
  http://purl.obolibrary.org/obo/MP_0005039

文献

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

• Jun. Ren, et.al., Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/12629158