abnormal object recognition memory_Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0

http://metadb.riken.jp/0001458I129C57BL6C57BL6JC57BL6NSJLSlc6a8tm11LbarYTgNescre1Kln0TgNescre1KlnSlc6a8tm11Lbar

abnormal object recognition memory_Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0

表現型アノテーション

MGI marker

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

• solute carrier family 6 (neurotransmitter transporter, creatine), member 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:2147834
• transgene insertion 1, Rudiger Klein
  http://metadb.riken.jp/db/mgi_rdf/MGI:2176172

遺伝子型

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

• Slc6a8<tm1.1Lbar>/Y,Tg(Nes-cre)1Kln/0

アレルシンボル

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

• Tg(Nes-cre)1Kln|Slc6a8<tm1.1Lbar>

遺伝的背景

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

• involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL

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

• Laura. Baroncelli, et.al., A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain aging., Human molecular genetics, 2016, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/27466184