hindlimb paralysis_Ugt8a<tm1Wst>/Ugt8a<tm1Wst>

http://metadb.riken.jp/0000755I129S1Sv129X1SvJC57BL6Ugt8atm1WstUgt8atm1WstUgt8atm1Wst

hindlimb paralysis_Ugt8a<tm1Wst>/Ugt8a<tm1Wst>

表現型アノテーション

MGI marker

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

• UDP galactosyltransferase 8A
  http://metadb.riken.jp/db/mgi_rdf/MGI:109522

遺伝子型

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

• Ugt8a<tm1Wst>/Ugt8a<tm1Wst>

アレルシンボル

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

• Ugt8a<tm1Wst>

遺伝的背景

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

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

MP annotation

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

• hindlimb paralysis
  http://purl.obolibrary.org/obo/MP_0000755

文献

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

• A. Bosio, et.al., Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis., Proceedings of the National Academy of Sciences of the United States of America, 1996, 93
  http://rdf.ncbi.nlm.nih.gov/pubmed/8917582