blind ureter_Fmn1<tm1Awb>/Fmn1<tm1Awb>

http://metadb.riken.jp/0011797I129S4SvJaeNIHBlackSwissFmn1tm1AwbFmn1tm1AwbFmn1tm1Awb

blind ureter_Fmn1<tm1Awb>/Fmn1<tm1Awb>

表現型アノテーション

MGI marker

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

• formin 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:101815

遺伝子型

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

• Fmn1<tm1Awb>/Fmn1<tm1Awb>

アレルシンボル

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

• Fmn1<tm1Awb>

遺伝的背景

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

• involves: 129S4/SvJae * NIH Black Swiss

MP annotation

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

• blind ureter
  http://purl.obolibrary.org/obo/MP_0011797

文献

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

• A. Wynshaw-Boris, et.al., The role of a single formin isoform in the limb and renal phenotypes of limb deformity., Molecular medicine (Cambridge, Mass.), 1997, 3
  http://rdf.ncbi.nlm.nih.gov/pubmed/9234242