abnormal eye movement_Grid2<ho-15J>/Grid2<ho-15J>

http://metadb.riken.jp/0001389IC3HeBFeGrid2ho15JGrid2ho15JGrid2ho15J

abnormal eye movement_Grid2<ho-15J>/Grid2<ho-15J>

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<ho-15J>/Grid2<ho-15J>

アレルシンボル

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

• Grid2<ho-15J>

遺伝的背景

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

• involves: C3HeB/Fe

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