absent cochlea_Hoxa1<tm1Ipc>/Hoxa1<tm1Ipc>

http://metadb.riken.jp/0003147I129S2SvPasC57BL6Hoxa1tm1IpcHoxa1tm1IpcHoxa1tm1Ipc

absent cochlea_Hoxa1<tm1Ipc>/Hoxa1<tm1Ipc>

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

遺伝子型

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

• Hoxa1<tm1Ipc>/Hoxa1<tm1Ipc>

アレルシンボル

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

• Hoxa1<tm1Ipc>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6

MP annotation

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

• absent cochlea
  http://purl.obolibrary.org/obo/MP_0003147

文献

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

• T. Lufkin, et.al., Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression., Cell, 1991, 66
  http://rdf.ncbi.nlm.nih.gov/pubmed/1680563
• M. Pasqualetti, et.al., Retinoic acid rescues inner ear defects in Hoxa1 deficient mice., Nature genetics, 2001, 29
  http://rdf.ncbi.nlm.nih.gov/pubmed/11528388