axon degeneration_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>

http://metadb.riken.jp/0005405I129S1Sv129X1SvJBALBcJC57BL6Zfyve26tm11CahbZfyve26tm11CahbZfyve26tm11Cahb

axon degeneration_Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>

表現型アノテーション

MGI marker

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

• zinc finger, FYVE domain containing 26
  http://metadb.riken.jp/db/mgi_rdf/MGI:1924767

遺伝子型

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

• Zfyve26<tm1.1Cahb>/Zfyve26<tm1.1Cahb>

アレルシンボル

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

• Zfyve26<tm1.1Cahb>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6

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

• 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