abnormal PNS synaptic transmission_Chrne<tm2Vwi>/Chrne<tm2Vwi>

http://metadb.riken.jp/0002913I129P2OlaHsdC57BL6Chrnetm2VwiChrnetm2VwiChrnetm2Vwi

abnormal PNS synaptic transmission_Chrne<tm2Vwi>/Chrne<tm2Vwi>

表現型アノテーション

MGI marker

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

• cholinergic receptor, nicotinic, epsilon polypeptide
  http://metadb.riken.jp/db/mgi_rdf/MGI:87894

遺伝子型

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

• Chrne<tm2Vwi>/Chrne<tm2Vwi>

アレルシンボル

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

• Chrne<tm2Vwi>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal PNS synaptic transmission
  http://purl.obolibrary.org/obo/MP_0002913

文献

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

• Frédéric. Chevessier, et.al., A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation., Neurobiology of disease, 2012, 45
  http://rdf.ncbi.nlm.nih.gov/pubmed/22178625