paraparesis_Psap<tm3.1Ggb>/Psap<tm3.1Ggb>

http://metadb.riken.jp/0009434I129SSvEvC57BL6JPsaptm31GgbPsaptm31GgbPsaptm31Ggb

paraparesis_Psap<tm3.1Ggb>/Psap<tm3.1Ggb>

表現型アノテーション

MGI marker

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

• prosaposin
  http://metadb.riken.jp/db/mgi_rdf/MGI:97783

遺伝子型

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

• Psap<tm3.1Ggb>/Psap<tm3.1Ggb>

アレルシンボル

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

• Psap<tm3.1Ggb>

遺伝的背景

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

• involves: 129S/SvEv * C57BL/6J

MP annotation

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

• paraparesis
  http://purl.obolibrary.org/obo/MP_0009434

文献

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

• Ying. Sun, et.al., Specific saposin C deficiency: CNS impairment and acid beta-glucosidase effects in the mouse., Human molecular genetics, 2010, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/20015957