no abnormal phenotype detected_Emx1<tm1(cre)Krj>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>

http://metadb.riken.jp/0002169EI129S1Sv129S2SvPasC57BL6orI129S1Sv129S2SvPas129X1SvJC57BL6Emx1tm1creKrjRai1tm21LuoRai1tm21LuoEmx1tm1creKrjRai1tm21Luo

no abnormal phenotype detected_Emx1<tm1(cre)Krj>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>

表現型アノテーション

MGI marker

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

• retinoic acid induced 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:103291
• empty spiracles homeobox 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:95387

遺伝子型

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

• Emx1<tm1(cre)Krj>/?,Rai1<tm2.1Luo>/Rai1<tm2.1Luo>

アレルシンボル

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

• Emx1<tm1(cre)Krj>|Rai1<tm2.1Luo>

遺伝的背景

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

• either: (involves: 129S1/Sv * 129S2/SvPas * C57BL/6) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6)

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