hypoactivity_Scn8a<9J>/Scn8a<+>

http://metadb.riken.jp/0001402B6JCScn8a9JMmScn8a9JScn8aScn8a9JScn8a

hypoactivity_Scn8a<9J>/Scn8a<+>

表現型アノテーション

MGI marker

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

• sodium channel, voltage-gated, type VIII, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:103169

遺伝子型

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

• Scn8a<9J>/Scn8a<+>

アレルシンボル

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

• Scn8a<9J>|Scn8a<+>

遺伝的背景

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

• B6J.C-Scn8a<9J>/Mm

MP annotation

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

• hypoactivity
  http://purl.obolibrary.org/obo/MP_0001402

文献

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

• Julie M. Jones, et.al., Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder., Neurobiology of disease, 2016, 89
  http://rdf.ncbi.nlm.nih.gov/pubmed/26807988