abnormal eye movement_Grid2<tm1(cre)Mwa>/Grid2<tm1(cre)Mwa>

http://metadb.riken.jp/0001389IC57BL6NGrid2tm1creMwaGrid2tm1creMwaGrid2tm1creMwa

abnormal eye movement_Grid2<tm1(cre)Mwa>/Grid2<tm1(cre)Mwa>

表現型アノテーション

MGI marker

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

• glutamate receptor, ionotropic, delta 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:95813

遺伝子型

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

• Grid2<tm1(cre)Mwa>/Grid2<tm1(cre)Mwa>

アレルシンボル

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

• Grid2<tm1(cre)Mwa>

遺伝的背景

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

• involves: C57BL/6N

MP annotation

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

• abnormal eye movement
  http://purl.obolibrary.org/obo/MP_0001389

文献

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

• L Benjamin. Hills, et.al., Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans., Neurology, 2013, 81
  http://rdf.ncbi.nlm.nih.gov/pubmed/24078737