abnormal muscle electrophysiology_Scn4a<m1Aaa>/Scn4a<+>

http://metadb.riken.jp/0004145IBALBcC57BL6JScn4am1AaaScn4aScn4am1AaaScn4a

abnormal muscle electrophysiology_Scn4a<m1Aaa>/Scn4a<+>

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 IV, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:98250

遺伝子型

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

• Scn4a<m1Aaa>/Scn4a<+>

アレルシンボル

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

• Scn4a<m1Aaa>|Scn4a<+>

遺伝的背景

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

• involves: BALB/c * C57BL/6J

MP annotation

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

• abnormal muscle electrophysiology
  http://purl.obolibrary.org/obo/MP_0004145

文献

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

• Silvia. Corrochano, et.al., Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis., Brain : a journal of neurology, 2014, 137
  http://rdf.ncbi.nlm.nih.gov/pubmed/25348630