abnormal involuntary movement_Itpr1<m1Asb>/Itpr1<opt>

http://metadb.riken.jp/0003492I129X1SvJC57BL6C57BLKSItpr1m1AsbItpr1optItpr1m1AsbItpr1opt

abnormal involuntary movement_Itpr1<m1Asb>/Itpr1<opt>

表現型アノテーション

MGI marker

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

• inositol 1,4,5-trisphosphate receptor 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:96623

遺伝子型

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

• Itpr1<m1Asb>/Itpr1<opt>

アレルシンボル

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

• Itpr1<m1Asb>|Itpr1<opt>

遺伝的背景

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

• involves: 129X1/SvJ * C57BL/6 * C57BLKS

MP annotation

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

• abnormal involuntary movement
  http://purl.obolibrary.org/obo/MP_0003492

文献

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

• Joyce. van de Leemput, et.al., Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans., PLoS genetics, 2007, 3
  http://rdf.ncbi.nlm.nih.gov/pubmed/17590087