abnormal nervous system electrophysiology_Pcmt1<tm1Shs>/Pcmt1<tm1Shs>

http://metadb.riken.jp/0002272I129P2OlaHsdC57BL6Pcmt1tm1ShsPcmt1tm1ShsPcmt1tm1Shs

abnormal nervous system electrophysiology_Pcmt1<tm1Shs>/Pcmt1<tm1Shs>

表現型アノテーション

MGI marker

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

• protein-L-isoaspartate (D-aspartate) O-methyltransferase 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:97502

遺伝子型

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

• Pcmt1<tm1Shs>/Pcmt1<tm1Shs>

アレルシンボル

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

• Pcmt1<tm1Shs>

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 nervous system electrophysiology
  http://purl.obolibrary.org/obo/MP_0002272

文献

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

• A. Yamamoto, et.al., Deficiency in protein L-isoaspartyl methyltransferase results in a fatal progressive epilepsy., The Journal of neuroscience : the official journal of the Society for Neuroscience, 1998, 18
  http://rdf.ncbi.nlm.nih.gov/pubmed/9482793