abnormal axon morphology_Aga<tm1Vk>/Aga<tm1Vk>

http://metadb.riken.jp/0005404I129S1Sv129X1SvJBlackSwissAgatm1VkAgatm1VkAgatm1Vk

abnormal axon morphology_Aga<tm1Vk>/Aga<tm1Vk>

表現型アノテーション

MGI marker

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

• aspartylglucosaminidase
  http://metadb.riken.jp/db/mgi_rdf/MGI:104873

遺伝子型

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

• Aga<tm1Vk>/Aga<tm1Vk>

アレルシンボル

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

• Aga<tm1Vk>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * Black Swiss

MP annotation

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

• abnormal axon morphology
  http://purl.obolibrary.org/obo/MP_0005404

文献

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

• V. Kaartinen, et.al., A mouse model for the human lysosomal disease aspartylglycosaminuria., Nature medicine, 1996, 2
  http://rdf.ncbi.nlm.nih.gov/pubmed/8946839