microphthalmia_Frem1<eyes2>/Frem1<eyes2>

http://metadb.riken.jp/0001297I129S6SvEvTacC57BL6JFrem1eyes2Frem1eyes2Frem1eyes2

microphthalmia_Frem1<eyes2>/Frem1<eyes2>

表現型アノテーション

MGI marker

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

• Fras1 related extracellular matrix protein 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2670972

遺伝子型

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

• Frem1<eyes2>/Frem1<eyes2>

アレルシンボル

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

• Frem1<eyes2>

遺伝的背景

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

• involves: 129S6/SvEvTac * 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

• Tyler F. Beck, et.al., Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23221805