no abnormal phenotype detected_Kif5a<tm1.1Noh>/Kif5a<tm1.2Noh>

http://metadb.riken.jp/0002169I129S6SvEvTacC57BL6C57BL6JCBAKif5atm11NohKif5atm12NohKif5atm11NohKif5atm12Noh

no abnormal phenotype detected_Kif5a<tm1.1Noh>/Kif5a<tm1.2Noh>

表現型アノテーション

MGI marker

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

• kinesin family member 5A
  http://metadb.riken.jp/db/mgi_rdf/MGI:109564

遺伝子型

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

• Kif5a<tm1.1Noh>/Kif5a<tm1.2Noh>

アレルシンボル

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

• Kif5a<tm1.1Noh>|Kif5a<tm1.2Noh>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Kazuo. Nakajima, et.al., Molecular motor KIF5A is essential for GABA(A) receptor transport, and KIF5A deletion causes epilepsy., Neuron, 2012, 76
  http://rdf.ncbi.nlm.nih.gov/pubmed/23217743