deafness_Slc12a2<sy-ns>/Slc12a2<sy-ns>

http://metadb.riken.jp/0001967IC57BL6MKReJSlc12a2synsSlc12a2synsSlc12a2syns

deafness_Slc12a2<sy-ns>/Slc12a2<sy-ns>

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<sy-ns>/Slc12a2<sy-ns>

アレルシンボル

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

• Slc12a2<sy-ns>

遺伝的背景

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

• involves: C57BL/6 * MK/ReJ

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

• K R. Johnson, et.al., The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome., Mammalian genome : official journal of the International Mammalian Genome Society, 1998, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/9799839