Junko. Matsuda, et.al., Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse., Human molecular genetics, 2004, 13

http://rdf.ncbi.nlm.nih.gov/pubmed/15345707

Junko. Matsuda, et.al., Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse., Human molecular genetics, 2004, 13

pubmed

BRC マウスの系統

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

• Saposin D mutant mouse
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC01293

表現型アノテーション

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

• hydronephrosis in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002415
• abnormal gait in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002421
• polyuria in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002424
• Purkinje cell degeneration in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002418
• abnormal motor coordination/ balance in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002423
• polydipsia in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002422
• abnormal kidney cortex morphology in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002416
• ataxia in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002420
• small cerebellum in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002417
• abnormal renal tubule morphology in RBRC01293
  http://metadb.riken.jp/db/rikenbrc_mouse/Phenotype_1002425

Class

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

• Saposin D mutant mouse
  http://metadb.riken.jp/db/rikenbrc_mouse/RBRC01293

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]

allele

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

• Psap<tm1Juma>
  http://metadb.riken.jp/db/mgi_rdf/MGI:3521746

表現型アノテーション

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

• polyuria_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0001762I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• ataxia_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0001393I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• Purkinje cell degeneration_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0000876I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• abnormal motor coordination/ balance_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0001516I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• premature death_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0002083I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• abnormal renal tubule morphology_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0002703I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• abnormal gait_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0001406I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• hydronephrosis_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0000519I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• polydipsia_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0001426I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• abnormal kidney cortex morphology_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0000521I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma
• small cerebellum_Psap<tm1Juma>/Psap<tm1Juma>
  http://metadb.riken.jp/0000852I129SSvEvC57BL6JPsaptm1JumaPsaptm1JumaPsaptm1Juma

article

http://www.w3.org/2000/01/rdf-schema#seeAlso

• [Blank]