abnormal cone electrophysiology_Prph2<Nmf193>/Prph2<Nmf193>

http://metadb.riken.jp/0004022C57BL6JPrph2Nmf193Prph2Nmf193Prph2Nmf193Prph2Nmf193

abnormal cone electrophysiology_Prph2<Nmf193>/Prph2<Nmf193>

表現型アノテーション

MGI marker

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

• peripherin 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:102791

遺伝子型

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

• Prph2<Nmf193>/Prph2<Nmf193>

アレルシンボル

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

• Prph2<Nmf193>

遺伝的背景

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

• C57BL/6J-Prph2<Nmf193>

MP annotation

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

• abnormal cone electrophysiology
  http://purl.obolibrary.org/obo/MP_0004022

文献

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

• Arne M. Nystuen, et.al., A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas., Mammalian genome : official journal of the International Mammalian Genome Society, 2008, 19
  http://rdf.ncbi.nlm.nih.gov/pubmed/18763016