scoliosis_Spg7<tm1Eir>/Spg7<tm1Eir>

http://metadb.riken.jp/0000161E129SvSpg7tm1EirorI129SvC57BL6Spg7tm1EirSpg7tm1EirSpg7tm1Eir

scoliosis_Spg7<tm1Eir>/Spg7<tm1Eir>

表現型アノテーション

MGI marker

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

• SPG7, paraplegin matrix AAA peptidase subunit
  http://metadb.riken.jp/db/mgi_rdf/MGI:2385906

遺伝子型

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

• Spg7<tm1Eir>/Spg7<tm1Eir>

アレルシンボル

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

• Spg7<tm1Eir>

遺伝的背景

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

• either: 129/Sv-Spg7<tm1Eir> or (involves: 129/Sv * C57BL/6)

MP annotation

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

• scoliosis
  http://purl.obolibrary.org/obo/MP_0000161

文献

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

• Fatima. Ferreirinha, et.al., Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport., The Journal of clinical investigation, 2004, 113
  http://rdf.ncbi.nlm.nih.gov/pubmed/14722615