forelimb paralysis_Btd<tm1Bwol>/Btd<tm1Bwol>

http://metadb.riken.jp/0000756B6CgBtdtm1BwolBtdtm1BwolBtdtm1BwolBtdtm1Bwol

forelimb paralysis_Btd<tm1Bwol>/Btd<tm1Bwol>

表現型アノテーション

MGI marker

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

• biotinidase
  http://metadb.riken.jp/db/mgi_rdf/MGI:1347001

遺伝子型

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

• Btd<tm1Bwol>/Btd<tm1Bwol>

アレルシンボル

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

• Btd<tm1Bwol>

遺伝的背景

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

• B6.Cg-Btd<tm1Bwol>

MP annotation

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

• forelimb paralysis
  http://purl.obolibrary.org/obo/MP_0000756

文献

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

• Kirit. Pindolia, et.al., Development and characterization of a mouse with profound biotinidase deficiency: a biotin-responsive neurocutaneous disorder., Molecular genetics and metabolism, 2011, 102
  http://rdf.ncbi.nlm.nih.gov/pubmed/21051254