deafness_Slc12a2<K842*>/Slc12a2<K842*>

http://metadb.riken.jp/0001967IFVBNSlc12a2K842Slc12a2K842Slc12a2K842

deafness_Slc12a2<K842*>/Slc12a2<K842*>

表現型アノテーション

MGI marker

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

• solute carrier family 12, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:101924

遺伝子型

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

• Slc12a2<K842*>/Slc12a2<K842*>

アレルシンボル

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

• Slc12a2<K842*>

遺伝的背景

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

• involves: FVB/N

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

• Michelle W. Antoine, et.al., A causative link between inner ear defects and long-term striatal dysfunction., Science (New York, N.Y.), 2013, 341
  http://rdf.ncbi.nlm.nih.gov/pubmed/24009395