abnormal axonal transport_Kif1b<tm1Noh>/Kif1b<+>

http://metadb.riken.jp/0004768I129S4SvJaeC57BL6JKif1btm1NohKif1bKif1bKif1btm1Noh

abnormal axonal transport_Kif1b<tm1Noh>/Kif1b<+>

表現型アノテーション

MGI marker

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

• kinesin family member 1B
  http://metadb.riken.jp/db/mgi_rdf/MGI:108426

遺伝子型

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

• Kif1b<tm1Noh>/Kif1b<+>

アレルシンボル

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

• Kif1b<+>|Kif1b<tm1Noh>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6J

MP annotation

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

• abnormal axonal transport
  http://purl.obolibrary.org/obo/MP_0004768

文献

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

• C. Zhao, et.al., Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta., Cell, 2001, 105
  http://rdf.ncbi.nlm.nih.gov/pubmed/11389829