abnormal gait_Fbxo41<tm1(KOMP)Vlcg>/Fbxo41<tm1(KOMP)Vlcg>

http://metadb.riken.jp/0001406IC57BL6NTacFbxo41tm1KOMPVlcgFbxo41tm1KOMPVlcgFbxo41tm1KOMPVlcg

abnormal gait_Fbxo41<tm1(KOMP)Vlcg>/Fbxo41<tm1(KOMP)Vlcg>

表現型アノテーション

MGI marker

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

• F-box protein 41
  http://metadb.riken.jp/db/mgi_rdf/MGI:1261912

遺伝子型

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

• Fbxo41<tm1(KOMP)Vlcg>/Fbxo41<tm1(KOMP)Vlcg>

アレルシンボル

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

• Fbxo41<tm1(KOMP)Vlcg>

遺伝的背景

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

• involves: C57BL/6NTac

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

• Chaitali. Mukherjee, et.al., Loss of the neuron-specific F-box protein FBXO41 models an ataxia-like phenotype in mice with neuronal migration defects and degeneration in the cerebellum., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015, 35
  http://rdf.ncbi.nlm.nih.gov/pubmed/26063905