abnormal object recognition memory_Slc6a8<tm1.2Lbar>/Y

http://metadb.riken.jp/0001458I129129S1SvC57BL6JC57BL6NSlc6a8tm12LbarYSlc6a8tm12Lbar

abnormal object recognition memory_Slc6a8<tm1.2Lbar>/Y

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

遺伝子型

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

• Slc6a8<tm1.2Lbar>/Y

アレルシンボル

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

• Slc6a8<tm1.2Lbar>

遺伝的背景

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

• involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N

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