microphthalmia_Hmx1<dmbo>/Hmx1<dmbo>

http://metadb.riken.jp/0001297IC3HeBFeJC57BL6JHmx1dmboHmx1dmboHmx1dmbo

microphthalmia_Hmx1<dmbo>/Hmx1<dmbo>

表現型アノテーション

MGI marker

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

• H6 homeobox 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:107178

遺伝子型

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

• Hmx1<dmbo>/Hmx1<dmbo>

アレルシンボル

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

• Hmx1<dmbo>

遺伝的背景

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

• involves: C3HeB/FeJ * C57BL/6J

MP annotation

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

• microphthalmia
  http://purl.obolibrary.org/obo/MP_0001297

文献

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

• Robert J. Munroe, et.al., Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass., BMC developmental biology, 2009, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/19379485