hyperactivity_Mid1<tm1Mero>/Y

http://metadb.riken.jp/0001399B6CgMid1tm1MeroMid1tm1MeroYMid1tm1Mero

hyperactivity_Mid1<tm1Mero>/Y

表現型アノテーション

MGI marker

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

• midline 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1100537

遺伝子型

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

• Mid1<tm1Mero>/Y

アレルシンボル

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

• Mid1<tm1Mero>

遺伝的背景

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

• B6.Cg-Mid1<tm1Mero>

MP annotation

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

• hyperactivity
  http://purl.obolibrary.org/obo/MP_0001399

文献

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

• Alessio. Lancioni, et.al., Lack of Mid1, the mouse ortholog of the Opitz syndrome gene, causes abnormal development of the anterior cerebellar vermis., The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010, 30
  http://rdf.ncbi.nlm.nih.gov/pubmed/20181585