impaired coordination_Rai1<tm2.1Luo>/Rai1<+>,Slc17a6<tm2(cre)Lowl>/?

http://metadb.riken.jp/0001405EI129S1Sv129S6SvEvTacC57BL6orI129S1Sv129S6SvEvTac129X1SvJC57BL6Rai1tm21LuoRai1Slc17a6tm2creLowlRai1Rai1tm21LuoSlc17a6tm2creLowl

impaired coordination_Rai1<tm2.1Luo>/Rai1<+>,Slc17a6<tm2(cre)Lowl>/?

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
• solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:2156052

遺伝子型

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

• Rai1<tm2.1Luo>/Rai1<+>,Slc17a6<tm2(cre)Lowl>/?

アレルシンボル

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

• Rai1<+>|Rai1<tm2.1Luo>|Slc17a6<tm2(cre)Lowl>

遺伝的背景

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

• either: (involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)

MP annotation

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

• impaired coordination
  http://purl.obolibrary.org/obo/MP_0001405

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