ataxia_Tg(Prnp-SNCA*A53T)23Mkle/0

http://metadb.riken.jp/0001393IC3HHeJC57BL6JTgPrnpSNCAA53T23Mkle0TgPrnpSNCAA53T23Mkle

ataxia_Tg(Prnp-SNCA*A53T)23Mkle/0

表現型アノテーション

MGI marker

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

• transgene insertion 23, Michael K Lee
  http://metadb.riken.jp/db/mgi_rdf/MGI:3574080

遺伝子型

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

• Tg(Prnp-SNCA*A53T)23Mkle/0

アレルシンボル

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

• Tg(Prnp-SNCA*A53T)23Mkle

遺伝的背景

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

• involves: C3H/HeJ * C57BL/6J

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

• Michael K. Lee, et.al., Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice., Proceedings of the National Academy of Sciences of the United States of America, 2002, 99
  http://rdf.ncbi.nlm.nih.gov/pubmed/12084935