retinal photoreceptor degeneration_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>

http://metadb.riken.jp/0008450I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst

retinal photoreceptor degeneration_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>

表現型アノテーション

MGI marker

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

• coiled-coil domain containing 66
  http://metadb.riken.jp/db/mgi_rdf/MGI:2443639

遺伝子型

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

• Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>

アレルシンボル

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

• Ccdc66<Gt(E021F10)Wrst>

遺伝的背景

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

• involves: 129P2/OlaHsd * C57BL/6N

MP annotation

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

• retinal photoreceptor degeneration
  http://purl.obolibrary.org/obo/MP_0008450

文献

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

• Wanda M. Gerding, et.al., Ccdc66 null mutation causes retinal degeneration and dysfunction., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21680557