no abnormal phenotype detected_Htt<tm3Mem>/Htt<tm3Mem>

http://metadb.riken.jp/0002169I129SSvEv129S1Sv129X1SvJCD1Htttm3MemHtttm3MemHtttm3Mem

no abnormal phenotype detected_Htt<tm3Mem>/Htt<tm3Mem>

表現型アノテーション

MGI marker

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

• huntingtin
  http://metadb.riken.jp/db/mgi_rdf/MGI:96067

遺伝子型

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

• Htt<tm3Mem>/Htt<tm3Mem>

アレルシンボル

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

• Htt<tm3Mem>

遺伝的背景

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

• involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * CD-1

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

• J K. White, et.al., Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion., Nature genetics, 1997, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/9398841