no abnormal phenotype detected_Scn1a<tm1Kea>/Scn1a<+>

http://metadb.riken.jp/0002169129S6SvEvTacScn1atm1KeaScn1atm1KeaScn1aScn1aScn1atm1Kea

no abnormal phenotype detected_Scn1a<tm1Kea>/Scn1a<+>

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 I, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:98246

遺伝子型

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

• Scn1a<tm1Kea>/Scn1a<+>

アレルシンボル

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

• Scn1a<+>|Scn1a<tm1Kea>

遺伝的背景

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

• 129S6/SvEvTac-Scn1a<tm1Kea>

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

• A R. Miller, et.al., Mapping genetic modifiers of survival in a mouse model of Dravet syndrome., Genes, brain, and behavior, 2014, 13
  http://rdf.ncbi.nlm.nih.gov/pubmed/24152123