scoliosis_Flnb<tm1Vshn>/Flnb<tm1Vshn>

http://metadb.riken.jp/0000161I129S6SvEvTacC57BL6Flnbtm1VshnFlnbtm1VshnFlnbtm1Vshn

scoliosis_Flnb<tm1Vshn>/Flnb<tm1Vshn>

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<tm1Vshn>/Flnb<tm1Vshn>

アレルシンボル

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

• Flnb<tm1Vshn>

遺伝的背景

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

• involves: 129S6/SvEvTac * 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

• Jie. Lu, et.al., Filamin B mutations cause chondrocyte defects in skeletal development., Human molecular genetics, 2007, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/17510210