deafness_Slc17a8<tm1Selm>/Slc17a8<tm1Selm>

http://metadb.riken.jp/0001967I129SvC57BL6Slc17a8tm1SelmSlc17a8tm1SelmSlc17a8tm1Selm

deafness_Slc17a8<tm1Selm>/Slc17a8<tm1Selm>

表現型アノテーション

MGI marker

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

• solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
  http://metadb.riken.jp/db/mgi_rdf/MGI:3039629

遺伝子型

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

• Slc17a8<tm1Selm>/Slc17a8<tm1Selm>

アレルシンボル

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

• Slc17a8<tm1Selm>

遺伝的背景

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

• involves: 129/Sv * C57BL/6

MP annotation

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

• deafness
  http://purl.obolibrary.org/obo/MP_0001967

文献

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

• Jérôme. Ruel, et.al., Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice., American journal of human genetics, 2008, 83
  http://rdf.ncbi.nlm.nih.gov/pubmed/18674745