no abnormal phenotype detected_Spast<tm1Jme>/Spast<tm1Jme>

http://metadb.riken.jp/0002169IC57BL6JSpasttm1JmeSpasttm1JmeSpasttm1Jme

no abnormal phenotype detected_Spast<tm1Jme>/Spast<tm1Jme>

表現型アノテーション

MGI marker

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

• spastin
  http://metadb.riken.jp/db/mgi_rdf/MGI:1858896

遺伝子型

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

• Spast<tm1Jme>/Spast<tm1Jme>

アレルシンボル

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

• Spast<tm1Jme>

遺伝的背景

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

• involves: C57BL/6J

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Anne. Tarrade, et.al., A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition., Human molecular genetics, 2006, 15
  http://rdf.ncbi.nlm.nih.gov/pubmed/17101632