ataxia_Psap<tm1Suz>/Psap<tm1Suz>

http://metadb.riken.jp/0001393I129P2OlaHsdPsaptm1SuzPsaptm1SuzPsaptm1Suz

ataxia_Psap<tm1Suz>/Psap<tm1Suz>

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<tm1Suz>/Psap<tm1Suz>

アレルシンボル

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

• Psap<tm1Suz>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• ataxia
  http://purl.obolibrary.org/obo/MP_0001393

文献

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

• N. Fujita, et.al., Targeted disruption of the mouse sphingolipid activator protein gene: a complex phenotype, including severe leukodystrophy and wide-spread storage of multiple sphingolipids., Human molecular genetics, 1996, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/8776585