abnormal cochlea morphology_Hoxa1<tm1Rez>/Hoxa1<tm1Rez>

http://metadb.riken.jp/0000031I129SSvEvBALBcC57BL6Hoxa1tm1RezHoxa1tm1RezHoxa1tm1Rez

abnormal cochlea morphology_Hoxa1<tm1Rez>/Hoxa1<tm1Rez>

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<tm1Rez>/Hoxa1<tm1Rez>

アレルシンボル

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

• Hoxa1<tm1Rez>

遺伝的背景

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

• involves: 129S/SvEv * BALB/c * C57BL/6

MP annotation

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

• abnormal cochlea morphology
  http://purl.obolibrary.org/obo/MP_0000031

文献

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

• Sophie. Remacle, et.al., Loss of function but no gain of function caused by amino acid substitutions in the hexapeptide of Hoxa1 in vivo., Molecular and cellular biology, 2004, 24
  http://rdf.ncbi.nlm.nih.gov/pubmed/15367676