deafness_Slc12a2<mpc246H>/Slc12a2<mpc246H>

http://metadb.riken.jp/0001967IBALBcC3HHeHC57BL6JSlc12a2mpc246HSlc12a2mpc246HSlc12a2mpc246H

deafness_Slc12a2<mpc246H>/Slc12a2<mpc246H>

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<mpc246H>/Slc12a2<mpc246H>

アレルシンボル

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

• Slc12a2<mpc246H>

遺伝的背景

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

• involves: BALB/c * C3H/HeH * C57BL/6J

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

• Paul K. Potter, et.al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease., Nature communications, 2016, 7
  http://rdf.ncbi.nlm.nih.gov/pubmed/27534441