axon degeneration_Psap<tm1Ggb>/Psap<tm1Ggb>

http://metadb.riken.jp/0005405I129SSvEvC57BL6JPsaptm1GgbPsaptm1GgbPsaptm1Ggb

axon degeneration_Psap<tm1Ggb>/Psap<tm1Ggb>

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<tm1Ggb>/Psap<tm1Ggb>

アレルシンボル

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

• Psap<tm1Ggb>

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

• axon degeneration
  http://purl.obolibrary.org/obo/MP_0005405

文献

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

• Ying. Sun, et.al., Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin trafficking., Human molecular genetics, 2007, 16
  http://rdf.ncbi.nlm.nih.gov/pubmed/17353235