no abnormal phenotype detected_Mnx1<tm4(cre)Tmj>/Mnx1<+>,Rhot1<tm1.1Jmsu>/Rhot1<tm1.2Jmsu>

http://metadb.riken.jp/0002169I129129S1SvC57BL6SJLMnx1tm4creTmjMnx1Rhot1tm11JmsuRhot1tm12JmsuRhot1tm11JmsuRhot1tm12JmsuMnx1Mnx1tm4creTmj

no abnormal phenotype detected_Mnx1<tm4(cre)Tmj>/Mnx1<+>,Rhot1<tm1.1Jmsu>/Rhot1<tm1.2Jmsu>

表現型アノテーション

MGI marker

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

• ras homolog family member T1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1926078
• motor neuron and pancreas homeobox 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:109160

遺伝子型

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

• Mnx1<tm4(cre)Tmj>/Mnx1<+>,Rhot1<tm1.1Jmsu>/Rhot1<tm1.2Jmsu>

アレルシンボル

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

• Rhot1<tm1.1Jmsu>|Rhot1<tm1.2Jmsu>|Mnx1<+>|Mnx1<tm4(cre)Tmj>

遺伝的背景

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

• involves: 129 * 129S1/Sv * C57BL/6 * SJL

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

• 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