no abnormal phenotype detected_Slc12a6<tm1Garo>/Slc12a6<tm1Garo>

http://metadb.riken.jp/0002169B6129Slc12a6tm1GaroSlc12a6tm1GaroSlc12a6tm1GaroSlc12a6tm1Garo

no abnormal phenotype detected_Slc12a6<tm1Garo>/Slc12a6<tm1Garo>

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<tm1Garo>/Slc12a6<tm1Garo>

アレルシンボル

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

• Slc12a6<tm1Garo>

遺伝的背景

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

• B6.129-Slc12a6<tm1Garo>

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Masoud. Shekarabi, et.al., Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012, 32
  http://rdf.ncbi.nlm.nih.gov/pubmed/22423107