abnormal gait_Kcnn2<fri>/Kcnn2<fri>

http://metadb.riken.jp/0001406IC3HKcnn2friKcnn2friKcnn2fri

abnormal gait_Kcnn2<fri>/Kcnn2<fri>

表現型アノテーション

MGI marker

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

• potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2153182

遺伝子型

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

• Kcnn2<fri>/Kcnn2<fri>

アレルシンボル

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

• Kcnn2<fri>

遺伝的背景

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

• involves: C3H

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

• N. Callizot, et.al., The frissonnant mutant mouse, a model of dopamino-sensitive, inherited motor syndrome., Neurobiology of disease, 2001, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/11442353