abnormal substantia nigra pars compacta morphology_Kcnj6<wv>/Kcnj6<+>

http://metadb.riken.jp/0013219IC57BL6JKcnj6wvKcnj6Kcnj6wvKcnj6

abnormal substantia nigra pars compacta morphology_Kcnj6<wv>/Kcnj6<+>

表現型アノテーション

MGI marker

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

• potassium inwardly-rectifying channel, subfamily J, member 6
  http://metadb.riken.jp/db/mgi_rdf/MGI:104781

遺伝子型

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

• Kcnj6<wv>/Kcnj6<+>

アレルシンボル

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

• Kcnj6<wv>|Kcnj6<+>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• abnormal substantia nigra pars compacta morphology
  http://purl.obolibrary.org/obo/MP_0013219

文献

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

• S. Signorini, et.al., Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2., Proceedings of the National Academy of Sciences of the United States of America, 1997, 94
  http://rdf.ncbi.nlm.nih.gov/pubmed/9023358