abnormal rod electrophysiology_Rho<tm1.1Kpal>/Rho<+>

http://metadb.riken.jp/0004021I129S6SvEvTacC57BL6FVBNRhotm11KpalRhoRhoRhotm11Kpal

abnormal rod electrophysiology_Rho<tm1.1Kpal>/Rho<+>

表現型アノテーション

MGI marker

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

• rhodopsin
  http://metadb.riken.jp/db/mgi_rdf/MGI:97914

遺伝子型

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

• Rho<tm1.1Kpal>/Rho<+>

アレルシンボル

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

• Rho<+>|Rho<tm1.1Kpal>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6 * FVB/N

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

• Sanae. Sakami, et.al., Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations., The Journal of biological chemistry, 2011, 286
  http://rdf.ncbi.nlm.nih.gov/pubmed/21224384