abnormal spatial learning_Kcnab2<tm1Kmc>/Kcnab2<tm1Kmc>

http://metadb.riken.jp/0001463I129S7SvEvBrdC57BL6Kcnab2tm1KmcKcnab2tm1KmcKcnab2tm1Kmc

abnormal spatial learning_Kcnab2<tm1Kmc>/Kcnab2<tm1Kmc>

表現型アノテーション

MGI marker

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

• potassium voltage-gated channel, shaker-related subfamily, beta member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:109239

遺伝子型

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

• Kcnab2<tm1Kmc>/Kcnab2<tm1Kmc>

アレルシンボル

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

• Kcnab2<tm1Kmc>

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

• abnormal spatial learning
  http://purl.obolibrary.org/obo/MP_0001463

文献

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

• John J. Perkowski, et.al., Deletion of the mouse homolog of KCNAB2, a gene linked to monosomy 1p36, results in associative memory impairments and amygdala hyperexcitability., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011, 31
  http://rdf.ncbi.nlm.nih.gov/pubmed/21209188