Mukhran. Khundadze, et.al., A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system., PLoS genetics, 2013, 9

http://rdf.ncbi.nlm.nih.gov/pubmed/24367272

Mukhran. Khundadze, et.al., A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system., PLoS genetics, 2013, 9

pubmed

allele

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

• Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5707975

表現型アノテーション

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

• astrocytosis_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0003354I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• enlarged urinary bladder_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0011874I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• abnormal gait_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0001406I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• abnormal posture_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0001504I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• decreased body weight_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0001262I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• axon degeneration_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0005405I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• ataxia_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0001393I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• abnormal urinary bladder physiology_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0010386I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• abnormal lysosome morphology_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0005058I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• decreased brain weight_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0002175I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• Purkinje cell degeneration_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0000876I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• brain atrophy_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0012506I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• kyphosis_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0000160I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• motor neuron degeneration_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0000938I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• impaired coordination_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0001405I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• abnormal lysosome physiology_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0003172I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb
• delayed axon extension_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/0002946I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb

class

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

• Zfyve26<tm1.1Cahb>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5707975