abnormal gait_Kcnma1<tm1Ruth>/Kcnma1<tm1Ruth>

http://metadb.riken.jp/0001406I129SvC57BL6Kcnma1tm1RuthKcnma1tm1RuthKcnma1tm1Ruth

abnormal gait_Kcnma1<tm1Ruth>/Kcnma1<tm1Ruth>

表現型アノテーション

MGI marker

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

• potassium large conductance calcium-activated channel, subfamily M, alpha member 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:99923

遺伝子型

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

• Kcnma1<tm1Ruth>/Kcnma1<tm1Ruth>

アレルシンボル

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

• Kcnma1<tm1Ruth>

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• M. Sausbier, et.al., Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiency., Proceedings of the National Academy of Sciences of the United States of America, 2004, 101
  http://rdf.ncbi.nlm.nih.gov/pubmed/15194823