no abnormal phenotype detected_Smn1<tm1Jme>/Smn1<tm1Jme>

http://metadb.riken.jp/0002169I129C57BL6JSmn1tm1JmeSmn1tm1JmeSmn1tm1Jme

no abnormal phenotype detected_Smn1<tm1Jme>/Smn1<tm1Jme>

表現型アノテーション

MGI marker

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

• survival motor neuron 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:109257

遺伝子型

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

• Smn1<tm1Jme>/Smn1<tm1Jme>

アレルシンボル

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

• Smn1<tm1Jme>

遺伝的背景

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

• involves: 129 * C57BL/6J

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

• T. Frugier, et.al., Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy., Human molecular genetics, 2000, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/10749994