abnormal cone electrophysiology_Rp2<tm1.2Asw>/Y

http://metadb.riken.jp/0004022I129SSvEvC57BL6Rp2tm12AswYRp2tm12Asw

abnormal cone electrophysiology_Rp2<tm1.2Asw>/Y

表現型アノテーション

MGI marker

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

• retinitis pigmentosa 2 homolog
  http://metadb.riken.jp/db/mgi_rdf/MGI:1277953

遺伝子型

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

• Rp2<tm1.2Asw>/Y

アレルシンボル

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

• Rp2<tm1.2Asw>

遺伝的背景

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

• involves: 129S/SvEv * C57BL/6

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

• Linjing. Li, et.al., Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration., Investigative ophthalmology & visual science, 2013, 54
  http://rdf.ncbi.nlm.nih.gov/pubmed/23745007