Subramaniam. Ganesh, et.al., Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice., Human molecular genetics, 2002, 11

http://rdf.ncbi.nlm.nih.gov/pubmed/12019206

Subramaniam. Ganesh, et.al., Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice., Human molecular genetics, 2002, 11

pubmed

allele

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

• Epm2a<tm1Kzy>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2182627

表現型アノテーション

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

• myoclonus_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0000243I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• muscle weakness_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0000747I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• increased neuron apoptosis_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0003203I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• impaired balance_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0001525I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• decreased grip strength_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0010053I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• axon degeneration_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0005405I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• abnormal brain wave pattern_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0004994I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• Lafora bodies_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0014063I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• hippocampal neuron degeneration_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0000811I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• Purkinje cell degeneration_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0000876I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• ataxia_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0001393I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• abnormal passive avoidance behavior_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0002799I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• impaired coordination_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0001405I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy
• increased startle reflex_Epm2a<tm1Kzy>/Epm2a<tm1Kzy>
  http://metadb.riken.jp/0001488I129P2OlaHsdC57BL6JEpm2atm1KzyEpm2atm1KzyEpm2atm1Kzy

class

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

• Epm2a<tm1Kzy>
  http://metadb.riken.jp/db/mgi_rdf/MGI:2182627

トランスクリプトームデータ

http://rdf.ncbi.nlm.nih.gov/pubmed/

• CD18792
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD18792

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]

BRC マウスの系統

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

• B6.129P2-Epm2a<tm1Kzy>
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC02715

表現型アノテーション

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

• myoclonus in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004915
• abnormal neuron morphology in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004932
• axon degeneration in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004942
• decreased grip strength in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004947
• abnormal passive avoidance behavior in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004931
• increased neuron apoptosis in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004934
• Purkinje cell degeneration in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004920
• increased startle reflex in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004925
• hippocampal neuron degeneration in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004919
• impaired coordination in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004923
• abnormal brain wave pattern in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004937
• ataxia in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004922
• impaired balance in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004926
• muscle weakness in RBRC02715
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1004918

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]