Braulio M. de Castro, et.al., The vesicular acetylcholine transporter is required for neuromuscular development and function., Molecular and cellular biology, 2009, 29

http://rdf.ncbi.nlm.nih.gov/pubmed/19635813

Braulio M. de Castro, et.al., The vesicular acetylcholine transporter is required for neuromuscular development and function., Molecular and cellular biology, 2009, 29

pubmed

allele

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

• Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4367609
• Chat/Slc18a3<tm1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4999563
• Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4367608
• Chat/Slc18a3<tm1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4999561

表現型アノテーション

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

• abnormal motor neuron innervation pattern_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0000940I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal synaptic acetylcholine release_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0004836I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• skeletal muscle atrophy_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0009417I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal neuromuscular synapse morphology_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0001053I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal neurotransmitter level_Chat/Slc18a3<tm1.1Vpra>/Chat<+>
  http://metadb.riken.jp/0002204I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatChatSlc18a3tm11VpraChat
• kyphosis_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0000160I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• increased motor neuron number_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0005192I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• neonatal lethality, complete penetrance_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0011087I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• hypotonia_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0004144I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal neurotransmitter level_Chat/Slc18a3<tm1.1Vpra>/Slc18a3<+>
  http://metadb.riken.jp/0002204I129S4SvJaeC57BL6JChatSlc18a3tm11VpraSlc18a3Slc18a3ChatSlc18a3tm11Vpra
• abnormal skeletal muscle morphology_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0000759I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• cyanosis_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0001575I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• skeletal muscle fiber atrophy_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0009413I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal miniature endplate potential_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0004835I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra
• abnormal neurotransmitter level_Chat/Slc18a3<tm1.1Vpra>/Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/0002204I129S4SvJaeC57BL6JChatSlc18a3tm11VpraChatSlc18a3tm11VpraChatSlc18a3tm11Vpra

class

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

• Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4367609
• Chat/Slc18a3<tm1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4999563
• Chat/Slc18a3<tm1.1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4367608
• Chat/Slc18a3<tm1Vpra>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4999561

トランスクリプトームデータ

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

• CD18686
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD18686