ataxia_Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0

http://metadb.riken.jp/0001393NSTgPrnpHTT82QKRT14EGFPC63Dbo0TgPrnpHTT82QKRT14EGFPC63Dbo

ataxia_Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0

表現型アノテーション

MGI marker

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

• transgene insertion C63, David R Borchelt
  http://metadb.riken.jp/db/mgi_rdf/MGI:5287242

遺伝子型

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

• Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo/0

アレルシンボル

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

• Tg(Prnp-HTT*82Q,KRT14-EGFP)C63Dbo

遺伝的背景

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

• Not Specified

MP annotation

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

• ataxia
  http://purl.obolibrary.org/obo/MP_0001393

文献

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

• Andrew T N. Tebbenkamp, et.al., Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivative., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21515588