no abnormal phenotype detected_Hoxa1<tm2Mrc>/Hoxa1<+>,Hoxa2<tm1Mrc>/Hoxa2<+>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJHoxa1tm2MrcHoxa1Hoxa2tm1MrcHoxa2Hoxa2Hoxa1tm2MrcHoxa1Hoxa2tm1Mrc

no abnormal phenotype detected_Hoxa1<tm2Mrc>/Hoxa1<+>,Hoxa2<tm1Mrc>/Hoxa2<+>

表現型アノテーション

MGI marker

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

• homeobox A1
  http://metadb.riken.jp/db/mgi_rdf/MGI:96170
• homeobox A2
  http://metadb.riken.jp/db/mgi_rdf/MGI:96174

遺伝子型

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

• Hoxa1<tm2Mrc>/Hoxa1<+>,Hoxa2<tm1Mrc>/Hoxa2<+>

アレルシンボル

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

• Hoxa2<+>|Hoxa1<tm2Mrc>|Hoxa1<+>|Hoxa2<tm1Mrc>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• J R. Barrow, et.al., Compensatory defects associated with mutations in Hoxa1 restore normal palatogenesis to Hoxa2 mutants., Development (Cambridge, England), 1999, 126
  http://rdf.ncbi.nlm.nih.gov/pubmed/10529419