holoprosencephaly_Foxq1<sa>/Foxq1<+>,M1073b/Del(13)36H

http://metadb.riken.jp/0005157I101BALBcOlaHsdC3HC57BL6JC57BRFoxq1saFoxq1M1073bDel1336HFoxq1saM1073bDel1336HFoxq1

holoprosencephaly_Foxq1<sa>/Foxq1<+>,M1073b/Del(13)36H

表現型アノテーション

MGI marker

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

• mutant 1073b
  http://metadb.riken.jp/db/mgi_rdf/MGI:5515454
• forkhead box Q1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1298228
• 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

• Foxq1<sa>/Foxq1<+>,M1073b/Del(13)36H

アレルシンボル

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

• Foxq1<sa>|M1073b|Del(13)36H|+|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

• holoprosencephaly
  http://purl.obolibrary.org/obo/MP_0005157

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