abnormal eye development_sau/Del(13)36H,Foxq1<sa>/Foxq1<+>

http://metadb.riken.jp/0001286I101BALBcOlaHsdC3HC57BL6JC57BRsauDel1336HFoxq1saFoxq1Foxq1saDel1336HsauFoxq1

abnormal eye development_sau/Del(13)36H,Foxq1<sa>/Foxq1<+>

表現型アノテーション

MGI marker

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

• forkhead box Q1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1298228
• sauron
  http://metadb.riken.jp/db/mgi_rdf/MGI:3607718
• deletion, Chr 13, Harwell 36
  http://metadb.riken.jp/db/mgi_rdf/MGI:104137

遺伝子型

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

• sau/Del(13)36H,Foxq1<sa>/Foxq1<+>

アレルシンボル

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

• Foxq1<sa>|Del(13)36H|+|sau|Foxq1<+>

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

• abnormal eye development
  http://purl.obolibrary.org/obo/MP_0001286

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