abnormal spatial learning_Ndn<tm1.1Mus>/Ndn<+>

http://metadb.riken.jp/0001463I129S2SvPasC57BL6JNdntm11MusNdnNdnNdntm11Mus

abnormal spatial learning_Ndn<tm1.1Mus>/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<tm1.1Mus>/Ndn<+>

アレルシンボル

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

• Ndn<+>|Ndn<tm1.1Mus>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6J

MP annotation

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

• abnormal spatial learning
  http://purl.obolibrary.org/obo/MP_0001463

文献

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

• F. Muscatelli, et.al., Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome., Human molecular genetics, 2000, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/11115855