no abnormal phenotype detected_Tg(ACTA1-SMN)69Ahmb/0

http://metadb.riken.jp/0002169IFVBNTgACTA1SMN69Ahmb0TgACTA1SMN69Ahmb

no abnormal phenotype detected_Tg(ACTA1-SMN)69Ahmb/0

表現型アノテーション

MGI marker

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

• transgene insertion 69, Arthur H M Burghes
  http://metadb.riken.jp/db/mgi_rdf/MGI:3774941

遺伝子型

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

• Tg(ACTA1-SMN)69Ahmb/0

アレルシンボル

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

• Tg(ACTA1-SMN)69Ahmb

遺伝的背景

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

• involves: FVB/N

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

• Tatiana O. Gavrilina, et.al., Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect., Human molecular genetics, 2008, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/18178576