ataxia_Arcn1<nur17>/Arcn1<nur17>

http://metadb.riken.jp/0001393I129S1SvImJ129S6SvEvTacC57BL6JArcn1nur17Arcn1nur17Arcn1nur17

ataxia_Arcn1<nur17>/Arcn1<nur17>

表現型アノテーション

MGI marker

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

• archain 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2387591

遺伝子型

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

• Arcn1<nur17>/Arcn1<nur17>

アレルシンボル

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

• Arcn1<nur17>

遺伝的背景

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

• involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6J

MP annotation

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

• ataxia
  http://purl.obolibrary.org/obo/MP_0001393

文献

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

• Xinjie. Xu, et.al., Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration., PLoS genetics, 2010, 6
  http://rdf.ncbi.nlm.nih.gov/pubmed/20502676