abnormal skeleton development_Sox9<tm1.1Gsr>/Sox9<+>

http://metadb.riken.jp/0002113I129P2OlaHsdC57BL6Sox9tm11GsrSox9Sox9tm11GsrSox9

abnormal skeleton development_Sox9<tm1.1Gsr>/Sox9<+>

表現型アノテーション

MGI marker

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

• SRY (sex determining region Y)-box 9
  http://metadb.riken.jp/db/mgi_rdf/MGI:98371

遺伝子型

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

• Sox9<tm1.1Gsr>/Sox9<+>

アレルシンボル

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

• Sox9<tm1.1Gsr>|Sox9<+>

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

• abnormal skeleton development
  http://purl.obolibrary.org/obo/MP_0002113

文献

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

• Ralf. Kist, et.al., Conditional inactivation of Sox9: a mouse model for campomelic dysplasia., Genesis (New York, N.Y. : 2000), 2002, 32
  http://rdf.ncbi.nlm.nih.gov/pubmed/11857796