failure of chorioallantoic fusion_M1616b/Del(13)36H,Foxq1<sa>/Foxq1<+>

http://metadb.riken.jp/0009657I101BALBcOlaHsdC3HC57BL6JC57BRM1616bDel1336HFoxq1saFoxq1Del1336HFoxq1saFoxq1M1616b

failure of chorioallantoic fusion_M1616b/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

• mutant 1616b
  http://metadb.riken.jp/db/mgi_rdf/MGI:5515460
• deletion, Chr 13, Harwell 36
  http://metadb.riken.jp/db/mgi_rdf/MGI:104137
• 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

• M1616b/Del(13)36H,Foxq1<sa>/Foxq1<+>

アレルシンボル

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

• Del(13)36H|Foxq1<sa>|+|Foxq1<+>|M1616b

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

• failure of chorioallantoic fusion
  http://purl.obolibrary.org/obo/MP_0009657

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