no abnormal phenotype detected_Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Gfap-cre)73.12Mvs/?

http://metadb.riken.jp/0002169EI129S1SvBALBcC57BL6C57BL6NHsdorI129S1Sv129X1SvJBALBcC57BL6C57BL6NHsdRai1tm21LuoRai1tm21LuoTgGfapcre7312MvsRai1tm21LuoTgGfapcre7312Mvs

no abnormal phenotype detected_Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Gfap-cre)73.12Mvs/?

表現型アノテーション

MGI marker

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

• transgene insertion 73.12, Michael V Sofroniew
  http://metadb.riken.jp/db/mgi_rdf/MGI:3522207
• retinoic acid induced 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:103291

遺伝子型

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

• Rai1<tm2.1Luo>/Rai1<tm2.1Luo>,Tg(Gfap-cre)73.12Mvs/?

アレルシンボル

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

• Rai1<tm2.1Luo>|Tg(Gfap-cre)73.12Mvs

遺伝的背景

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

• either: (involves: 129S1/Sv * BALB/c * C57BL/6 * C57BL/6NHsd) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6NHsd)

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

• Wei-Hsiang. Huang, et.al., Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome., Neuron, 2016, 92
  http://rdf.ncbi.nlm.nih.gov/pubmed/27693255