abnormal vitelline vascular remodeling_Sox7<tm1.1Dsco>/Sox7<tm1.1Dsco>

http://metadb.riken.jp/0004076I129SvEvC57BL6Sox7tm11DscoSox7tm11DscoSox7tm11Dsco

abnormal vitelline vascular remodeling_Sox7<tm1.1Dsco>/Sox7<tm1.1Dsco>

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 7
  http://metadb.riken.jp/db/mgi_rdf/MGI:98369

遺伝子型

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

• Sox7<tm1.1Dsco>/Sox7<tm1.1Dsco>

アレルシンボル

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

• Sox7<tm1.1Dsco>

遺伝的背景

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

• involves: 129/SvEv * C57BL/6

MP annotation

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

• abnormal vitelline vascular remodeling
  http://purl.obolibrary.org/obo/MP_0004076

文献

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

• Margaret J. Wat, et.al., Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22723016