abnormal artery development_Ccm2<tm1Sbn>/Ccm2<tm1Sbn>

http://metadb.riken.jp/0003410IC57BL6Ccm2tm1SbnCcm2tm1SbnCcm2tm1Sbn

abnormal artery development_Ccm2<tm1Sbn>/Ccm2<tm1Sbn>

表現型アノテーション

MGI marker

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

• cerebral cavernous malformation 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2384924

遺伝子型

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

• Ccm2<tm1Sbn>/Ccm2<tm1Sbn>

アレルシンボル

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

• Ccm2<tm1Sbn>

遺伝的背景

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

• involves: C57BL/6

MP annotation

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

• abnormal artery development
  http://purl.obolibrary.org/obo/MP_0003410

文献

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

• Kirk. Cunningham, et.al., Conditional deletion of Ccm2 causes hemorrhage in the adult brain: a mouse model of human cerebral cavernous malformations., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21596842