neuronal intranuclear inclusions_Fmr1<tm2Cgr>/Y

http://metadb.riken.jp/0004191I129P2OlaHsdFmr1tm2CgrYFmr1tm2Cgr

neuronal intranuclear inclusions_Fmr1<tm2Cgr>/Y

表現型アノテーション

MGI marker

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

• fragile X mental retardation syndrome 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95564

遺伝子型

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

• Fmr1<tm2Cgr>/Y

アレルシンボル

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

• Fmr1<tm2Cgr>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• neuronal intranuclear inclusions
  http://purl.obolibrary.org/obo/MP_0004191

文献

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

• Rob. Willemsen, et.al., The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome., Human molecular genetics, 2003, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/12700164