muscle hypertonia_Slc12a6<tm1Tjj>/Slc12a6<tm1Tjj>

http://metadb.riken.jp/0004143I129SvC57BL6Slc12a6tm1TjjSlc12a6tm1TjjSlc12a6tm1Tjj

muscle hypertonia_Slc12a6<tm1Tjj>/Slc12a6<tm1Tjj>

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<tm1Tjj>/Slc12a6<tm1Tjj>

アレルシンボル

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

• Slc12a6<tm1Tjj>

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

• muscle hypertonia
  http://purl.obolibrary.org/obo/MP_0004143

文献

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

• Thomas. Boettger, et.al., Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold., The EMBO journal, 2003, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/14532115