abnormal object recognition memory_Dp(16Cbr1-Fam3b)1Rhr/0

http://metadb.riken.jp/0001458I129S6SvEvTacC3HHeSnJC57BL6EiDp16Cbr1Fam3b1Rhr0Dp16Cbr1Fam3b1Rhr

abnormal object recognition memory_Dp(16Cbr1-Fam3b)1Rhr/0

表現型アノテーション

MGI marker

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

• duplication, Chr 16, H R Reeves 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:3487250

遺伝子型

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

• Dp(16Cbr1-Fam3b)1Rhr/0

アレルシンボル

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

• Dp(16Cbr1-Fam3b)1Rhr

遺伝的背景

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

• involves: 129S6/SvEvTac * C3H/HeSnJ * C57BL/6Ei

MP annotation

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

• abnormal object recognition memory
  http://purl.obolibrary.org/obo/MP_0001458

文献

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

• Nadia P. Belichenko, et.al., The "Down syndrome critical region" is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndrome., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/19420260