axon degeneration_Abcd2<tm1Apuj>/Abcd2<tm1Apuj>

http://metadb.riken.jp/0005405I129S1Sv129X1SvJC57BL6JAbcd2tm1ApujAbcd2tm1ApujAbcd2tm1Apuj

axon degeneration_Abcd2<tm1Apuj>/Abcd2<tm1Apuj>

表現型アノテーション

MGI marker

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

• ATP-binding cassette, sub-family D (ALD), member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1349467

遺伝子型

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

• Abcd2<tm1Apuj>/Abcd2<tm1Apuj>

アレルシンボル

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

• Abcd2<tm1Apuj>

遺伝的背景

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

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

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

• Isidre. Ferrer, et.al., Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage., Human molecular genetics, 2005, 14
  http://rdf.ncbi.nlm.nih.gov/pubmed/16223892
• Aurora. Pujol, et.al., Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy., Human molecular genetics, 2004, 13
  http://rdf.ncbi.nlm.nih.gov/pubmed/15489218