scoliosis_Flnb<Gt(RRF239)Byg>/Flnb<Gt(RRF239)Byg>

http://metadb.riken.jp/0000161I129P2OlaHsdC57BL6FlnbGtRRF239BygFlnbGtRRF239BygFlnbGtRRF239Byg

scoliosis_Flnb<Gt(RRF239)Byg>/Flnb<Gt(RRF239)Byg>

表現型アノテーション

MGI marker

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

• filamin, beta
  http://metadb.riken.jp/db/mgi_rdf/MGI:2446089

遺伝子型

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

• Flnb<Gt(RRF239)Byg>/Flnb<Gt(RRF239)Byg>

アレルシンボル

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

• Flnb<Gt(RRF239)Byg>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6

MP annotation

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

• scoliosis
  http://purl.obolibrary.org/obo/MP_0000161

文献

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

• Claire. Farrington-Rock, et.al., Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome., Human molecular genetics, 2008, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/17635842