abnormal cerebellum development_Ntrk2<tm1Bbd>/Ntrk2<tm1Bbd>

http://metadb.riken.jp/0000854I129S2SvPasNtrk2tm1BbdNtrk2tm1BbdNtrk2tm1Bbd

abnormal cerebellum development_Ntrk2<tm1Bbd>/Ntrk2<tm1Bbd>

表現型アノテーション

MGI marker

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

• neurotrophic tyrosine kinase, receptor, type 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:97384

遺伝子型

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

• Ntrk2<tm1Bbd>/Ntrk2<tm1Bbd>

アレルシンボル

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

• Ntrk2<tm1Bbd>

遺伝的背景

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

• involves: 129S2/SvPas

MP annotation

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

• abnormal cerebellum development
  http://purl.obolibrary.org/obo/MP_0000854

文献

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

• L. Minichiello, et.al., Point mutation in trkB causes loss of NT4-dependent neurons without major effects on diverse BDNF responses., Neuron, 1998, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/9728915