abnormal motor capabilities/coordination/movement_Tg(ACTA1-cre/ERT2)97.16Mtz/0,Tg(CAG-DMPK*)1323Coop/0

http://metadb.riken.jp/0002066IFVBTgACTA1creERT29716Mtz0TgCAGDMPK1323Coop0TgACTA1creERT29716MtzTgCAGDMPK1323Coop

abnormal motor capabilities/coordination/movement_Tg(ACTA1-cre/ERT2)97.16Mtz/0,Tg(CAG-DMPK*)1323Coop/0

表現型アノテーション

MGI marker

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

• transgene insertion 97.16, Daniel Metzger
  http://metadb.riken.jp/db/mgi_rdf/MGI:3576656
• transgene insertion 1323, Thomas A Cooper
  http://metadb.riken.jp/db/mgi_rdf/MGI:5426789

遺伝子型

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

• Tg(ACTA1-cre/ERT2)97.16Mtz/0,Tg(CAG-DMPK*)1323Coop/0

アレルシンボル

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

• Tg(ACTA1-cre/ERT2)97.16Mtz|Tg(CAG-DMPK*)1323Coop

遺伝的背景

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

• involves: FVB

MP annotation

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

• abnormal motor capabilities/coordination/movement
  http://purl.obolibrary.org/obo/MP_0002066

文献

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

• James P. Orengo, et.al., Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy., Proceedings of the National Academy of Sciences of the United States of America, 2008, 105
  http://rdf.ncbi.nlm.nih.gov/pubmed/18272483