abnormal motor capabilities/coordination/movement_Hprt<tm1Detl>/Y

http://metadb.riken.jp/0002066I129S1Sv129X1SvJC57BL6JHprttm1DetlYHprttm1Detl

abnormal motor capabilities/coordination/movement_Hprt<tm1Detl>/Y

表現型アノテーション

MGI marker

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

• hypoxanthine guanine phosphoribosyl transferase
  http://metadb.riken.jp/db/mgi_rdf/MGI:96217

遺伝子型

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

• Hprt<tm1Detl>/Y

アレルシンボル

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

• Hprt<tm1Detl>

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

• abnormal motor capabilities/coordination/movement
  http://purl.obolibrary.org/obo/MP_0002066

文献

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

• J M. Ordway, et.al., Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse., Cell, 1997, 91
  http://rdf.ncbi.nlm.nih.gov/pubmed/9413985