no abnormal phenotype detected_Lmna<tm1Gbon>/Lmna<+>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6Lmnatm1GbonLmnaLmnaLmnatm1Gbon

no abnormal phenotype detected_Lmna<tm1Gbon>/Lmna<+>

表現型アノテーション

MGI marker

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

• lamin A
  http://metadb.riken.jp/db/mgi_rdf/MGI:96794

遺伝子型

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

• Lmna<tm1Gbon>/Lmna<+>

アレルシンボル

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

• Lmna<+>|Lmna<tm1Gbon>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6

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

• Takuro. Arimura, et.al., Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies., Human molecular genetics, 2005, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/15548545