no abnormal phenotype detected_Acvrl1<tm1Dyl>/Acvrl1<+>

http://metadb.riken.jp/0002169I129S1Sv129X1SvJC57BL6JAcvrl1tm1DylAcvrl1Acvrl1Acvrl1tm1Dyl

no abnormal phenotype detected_Acvrl1<tm1Dyl>/Acvrl1<+>

表現型アノテーション

MGI marker

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

• activin A receptor, type II-like 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1338946

遺伝子型

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

• Acvrl1<tm1Dyl>/Acvrl1<+>

アレルシンボル

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

• Acvrl1<+>|Acvrl1<tm1Dyl>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6J

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• L D. Urness, et.al., Arteriovenous malformations in mice lacking activin receptor-like kinase-1., Nature genetics, 2000, 26
  http://rdf.ncbi.nlm.nih.gov/pubmed/11062473
• Lise K. Sorensen, et.al., Loss of distinct arterial and venous boundaries in mice lacking endoglin, a vascular-specific TGFbeta coreceptor., Developmental biology, 2003, 261
  http://rdf.ncbi.nlm.nih.gov/pubmed/12941632