abnormal social investigation_Del(10Prmt2-Cstb)4Yah/+,Tc(HSA21)1TybEmcf/0

http://metadb.riken.jp/0001360I129P2OlaHsdBALBcC3HHeHC57BL6Del10Prmt2Cstb4YahTcHSA211TybEmcf0Del10Prmt2Cstb4YahTcHSA211TybEmcf

abnormal social investigation_Del(10Prmt2-Cstb)4Yah/+,Tc(HSA21)1TybEmcf/0

表現型アノテーション

MGI marker

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

• deletion, Chr10, Yann Herault 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:4868387
• transchromosomal, human 21, line 1, Victor Tybulewicz and Elizabeth M C Fisher
  http://metadb.riken.jp/db/mgi_rdf/MGI:3814702

遺伝子型

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

• Del(10Prmt2-Cstb)4Yah/+,Tc(HSA21)1TybEmcf/0

アレルシンボル

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

• Del(10Prmt2-Cstb)4Yah|+|Tc(HSA21)1TybEmcf

遺伝的背景

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

• involves: 129P2/OlaHsd * BALB/c * C3H/HeH * C57BL/6

MP annotation

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

• abnormal social investigation
  http://purl.obolibrary.org/obo/MP_0001360

文献

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

• Arnaud. Duchon, et.al., The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndrome., Behavioural brain research, 2011, 217
  http://rdf.ncbi.nlm.nih.gov/pubmed/21047530