hyperactivity_Foxq1<sa>/Foxq1<+>,M369b/+

http://metadb.riken.jp/0001399I101BALBcOlaHsdC3HC57BL6JC57BRFoxq1saFoxq1M369bFoxq1saFoxq1M369b

hyperactivity_Foxq1<sa>/Foxq1<+>,M369b/+

表現型アノテーション

MGI marker

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

• mutant 369b
  http://metadb.riken.jp/db/mgi_rdf/MGI:5515442
• forkhead box Q1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1298228

遺伝子型

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

• Foxq1<sa>/Foxq1<+>,M369b/+

アレルシンボル

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

• +|Foxq1<sa>|Foxq1<+>|M369b

遺伝的背景

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

• involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR

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

• Debora. Bogani, et.al., Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen., Proceedings of the National Academy of Sciences of the United States of America, 2005, 102
  http://rdf.ncbi.nlm.nih.gov/pubmed/16109771