seizures_Rai1<tm1Jrl>/Rai1<+>

http://metadb.riken.jp/0002064I129SSvEvBrdC57BL6Rai1tm1JrlRai1Rai1tm1JrlRai1

seizures_Rai1<tm1Jrl>/Rai1<+>

表現型アノテーション

MGI marker

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

• retinoic acid induced 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:103291

遺伝子型

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

• Rai1<tm1Jrl>/Rai1<+>

アレルシンボル

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

• Rai1<tm1Jrl>|Rai1<+>

遺伝的背景

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

• involves: 129S/SvEvBrd * C57BL/6

MP annotation

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

• seizures
  http://purl.obolibrary.org/obo/MP_0002064

文献

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

• Weimin. Bi, et.al., Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes., Human molecular genetics, 2007, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/17517686