abnormal rod electrophysiology_Tg(HDexon1)61Gpb/0

http://metadb.riken.jp/0004021IC57BL6CBAJTgHDexon161Gpb0TgHDexon161Gpb

abnormal rod electrophysiology_Tg(HDexon1)61Gpb/0

表現型アノテーション

MGI marker

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

• transgene insertion 61, Gillian Bates
  http://metadb.riken.jp/db/mgi_rdf/MGI:2653600

遺伝子型

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

• Tg(HDexon1)61Gpb/0

アレルシンボル

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

• Tg(HDexon1)61Gpb

遺伝的背景

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

• involves: C57BL/6 * CBA/J

MP annotation

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

• abnormal rod electrophysiology
  http://purl.obolibrary.org/obo/MP_0004021

文献

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

• Dominique. Helmlinger, et.al., Progressive retinal degeneration and dysfunction in R6 Huntington's disease mice., Human molecular genetics, 2002, 11
  http://rdf.ncbi.nlm.nih.gov/pubmed/12471061