abnormal voluntary movement_Scn8a<dmu>/Scn8a<med>

http://metadb.riken.jp/0003491IC3HC3HeBFeC57BL6Scn8admuScn8amedScn8amedScn8admu

abnormal voluntary movement_Scn8a<dmu>/Scn8a<med>

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<dmu>/Scn8a<med>

アレルシンボル

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

• Scn8a<med>|Scn8a<dmu>

遺伝的背景

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

• involves: C3H * C3HeB/Fe * C57BL/6

MP annotation

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

• abnormal voluntary movement
  http://purl.obolibrary.org/obo/MP_0003491

文献

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

• Y. De Repentigny, et.al., Pathological and genetic analysis of the degenerating muscle (dmu) mouse: a new allele of Scn8a., Human molecular genetics, 2001, 10
  http://rdf.ncbi.nlm.nih.gov/pubmed/11532991