abnormal gait_Atp13a2<tm1Pjsch>/Atp13a2<tm1Pjsch>

http://metadb.riken.jp/0001406I129S6SvEvTacBlackSwissAtp13a2tm1PjschAtp13a2tm1PjschAtp13a2tm1Pjsch

abnormal gait_Atp13a2<tm1Pjsch>/Atp13a2<tm1Pjsch>

表現型アノテーション

MGI marker

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

• ATPase type 13A2
  http://metadb.riken.jp/db/mgi_rdf/MGI:1922022

遺伝子型

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

• Atp13a2<tm1Pjsch>/Atp13a2<tm1Pjsch>

アレルシンボル

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

• Atp13a2<tm1Pjsch>

遺伝的背景

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

• involves: 129S6/SvEvTac * Black Swiss

MP annotation

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

• abnormal gait
  http://purl.obolibrary.org/obo/MP_0001406

文献

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

• Patrick J. Schultheis, et.al., Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits., Human molecular genetics, 2013, 22
  http://rdf.ncbi.nlm.nih.gov/pubmed/23393156