axon degeneration_Slc12a6<tm1Dlp>/Slc12a6<tm1Dlp>

http://metadb.riken.jp/0005405I129C57BL6JSlc12a6tm1DlpSlc12a6tm1DlpSlc12a6tm1Dlp

axon degeneration_Slc12a6<tm1Dlp>/Slc12a6<tm1Dlp>

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 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:2135960

遺伝子型

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

• Slc12a6<tm1Dlp>/Slc12a6<tm1Dlp>

アレルシンボル

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

• Slc12a6<tm1Dlp>

遺伝的背景

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

• involves: 129 * C57BL/6J

MP annotation

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

• axon degeneration
  http://purl.obolibrary.org/obo/MP_0005405

文献

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

• Heidi C. Howard, et.al., The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum., Nature genetics, 2002, 32
  http://rdf.ncbi.nlm.nih.gov/pubmed/12368912