no abnormal phenotype detected_Acvrl1<tm2.1Spo>/Acvrl1<tm2.1Spo>

http://metadb.riken.jp/0002169I129C57BL6FVBNAcvrl1tm21SpoAcvrl1tm21SpoAcvrl1tm21Spo

no abnormal phenotype detected_Acvrl1<tm2.1Spo>/Acvrl1<tm2.1Spo>

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<tm2.1Spo>/Acvrl1<tm2.1Spo>

アレルシンボル

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

• Acvrl1<tm2.1Spo>

遺伝的背景

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

• involves: 129 * C57BL/6 * FVB/N

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

• Sung O. Park, et.al., ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2., Blood, 2008, 111
  http://rdf.ncbi.nlm.nih.gov/pubmed/17911384