nuclear cataracts_Six5<tm1Rdd>/Six5<+>

http://metadb.riken.jp/0010254129S4SvJaeSix5tm1RddSix5tm1RddSix5Six5tm1RddSix5

nuclear cataracts_Six5<tm1Rdd>/Six5<+>

表現型アノテーション

MGI marker

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

• sine oculis-related homeobox 5
  http://metadb.riken.jp/db/mgi_rdf/MGI:106220

遺伝子型

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

• Six5<tm1Rdd>/Six5<+>

アレルシンボル

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

• Six5<tm1Rdd>|Six5<+>

遺伝的背景

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

• 129S4/SvJae-Six5<tm1Rdd>

MP annotation

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

• nuclear cataracts
  http://purl.obolibrary.org/obo/MP_0010254

文献

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

• P S. Sarkar, et.al., Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts., Nature genetics, 2000, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/10802668