myoclonus_Arx<tm1.1Jno>/Arx<tm1.1Jno>

http://metadb.riken.jp/0000243I129S7SvEvBrdC57BL6JArxtm11JnoArxtm11JnoArxtm11Jno

myoclonus_Arx<tm1.1Jno>/Arx<tm1.1Jno>

表現型アノテーション

MGI marker

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

• aristaless related homeobox
  http://metadb.riken.jp/db/mgi_rdf/MGI:1097716

遺伝子型

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

• Arx<tm1.1Jno>/Arx<tm1.1Jno>

アレルシンボル

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

• Arx<tm1.1Jno>

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6J

MP annotation

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

• myoclonus
  http://purl.obolibrary.org/obo/MP_0000243

文献

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

• Maureen G. Price, et.al., A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/19587282