abnormal social/conspecific interaction_Grin1<tm1.1Phs>/Grin1<+>

http://metadb.riken.jp/0002557I129S1Sv129X1SvJC57BL6Grin1tm11PhsGrin1Grin1Grin1tm11Phs

abnormal social/conspecific interaction_Grin1<tm1.1Phs>/Grin1<+>

表現型アノテーション

MGI marker

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

• glutamate receptor, ionotropic, NMDA1 (zeta 1)
  http://metadb.riken.jp/db/mgi_rdf/MGI:95819

遺伝子型

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

• Grin1<tm1.1Phs>/Grin1<+>

アレルシンボル

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

• Grin1<+>|Grin1<tm1.1Phs>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6

MP annotation

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

• abnormal social/conspecific interaction
  http://purl.obolibrary.org/obo/MP_0002557

文献

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

• F N. Single, et.al., Dysfunctions in mice by NMDA receptor point mutations NR1(N598Q) and NR1(N598R)., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2000, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/10729336