increased startle reflex_Del(11Cops3-Gid4)2Jrl/+

http://metadb.riken.jp/0001488I129S7SvEvBrdC57BL6Del11Cops3Gid42JrlDel11Cops3Gid42Jrl

increased startle reflex_Del(11Cops3-Gid4)2Jrl/+

表現型アノテーション

MGI marker

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

• deletion, Chr 11, James R Lupski 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:3521942

遺伝子型

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

• Del(11Cops3-Gid4)2Jrl/+

アレルシンボル

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

• +|Del(11Cops3-Gid4)2Jrl

遺伝的背景

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

• involves: 129S7/SvEvBrd * C57BL/6

MP annotation

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

• increased startle reflex
  http://purl.obolibrary.org/obo/MP_0001488

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