no abnormal phenotype detected_Tg(Thy1-GLRA1*R271Q)382Wha/0

http://metadb.riken.jp/0002169IC57BL6DBA2TgThy1GLRA1R271Q382Wha0TgThy1GLRA1R271Q382Wha

no abnormal phenotype detected_Tg(Thy1-GLRA1*R271Q)382Wha/0

表現型アノテーション

MGI marker

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

• transgene insertion 382, Hans Weiher
  http://metadb.riken.jp/db/mgi_rdf/MGI:5306913

遺伝子型

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

• Tg(Thy1-GLRA1*R271Q)382Wha/0

アレルシンボル

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

• Tg(Thy1-GLRA1*R271Q)382Wha

遺伝的背景

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

• involves: C57BL/6 * DBA/2

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

• Lore. Becker, et.al., Disease-specific human glycine receptor alpha1 subunit causes hyperekplexia phenotype and impaired glycine- and GABA(A)-receptor transmission in transgenic mice., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2002, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/11923415