abnormal tail movements_Rhot1<tm1.1Jmsu>/Rhot1<tm1.1Jmsu>,Tg(Eno2-cre)39Jme/0

http://metadb.riken.jp/0001391I129C57BL6C57BL6JSJLRhot1tm11JmsuRhot1tm11JmsuTgEno2cre39Jme0Rhot1tm11JmsuTgEno2cre39Jme

abnormal tail movements_Rhot1<tm1.1Jmsu>/Rhot1<tm1.1Jmsu>,Tg(Eno2-cre)39Jme/0

表現型アノテーション

MGI marker

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

• transgene insertion 39, Judith Melki
  http://metadb.riken.jp/db/mgi_rdf/MGI:2177174
• ras homolog family member T1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926078

遺伝子型

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

• Rhot1<tm1.1Jmsu>/Rhot1<tm1.1Jmsu>,Tg(Eno2-cre)39Jme/0

アレルシンボル

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

• Rhot1<tm1.1Jmsu>|Tg(Eno2-cre)39Jme

遺伝的背景

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

• involves: 129 * C57BL/6 * C57BL/6J * SJL

MP annotation

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

• abnormal tail movements
  http://purl.obolibrary.org/obo/MP_0001391

文献

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

• Tammy T. Nguyen, et.al., Loss of Miro1-directed mitochondrial movement results in a novel murine model for neuron disease., Proceedings of the National Academy of Sciences of the United States of America, 2014, 111
  http://rdf.ncbi.nlm.nih.gov/pubmed/25136135