malocclusion_Rai1<tm1Jrl>/Rai1<tm1Jrl>

http://metadb.riken.jp/0000120I129SSvEvBrdC57BL6Rai1tm1JrlRai1tm1JrlRai1tm1Jrl

malocclusion_Rai1<tm1Jrl>/Rai1<tm1Jrl>

表現型アノテーション

MGI marker

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

• retinoic acid induced 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:103291

遺伝子型

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

• Rai1<tm1Jrl>/Rai1<tm1Jrl>

アレルシンボル

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

• Rai1<tm1Jrl>

遺伝的背景

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

• involves: 129S/SvEvBrd * C57BL/6

MP annotation

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

• malocclusion
  http://purl.obolibrary.org/obo/MP_0000120

文献

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

• Weimin. Bi, et.al., Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome., Human molecular genetics, 2005, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/15746153