abnormal rod electrophysiology_Fscn2<tm1Sykk>/Fscn2<tm1Sykk>

http://metadb.riken.jp/0004021I129S4SvJaeC57BL6Fscn2tm1SykkFscn2tm1SykkFscn2tm1Sykk

abnormal rod electrophysiology_Fscn2<tm1Sykk>/Fscn2<tm1Sykk>

表現型アノテーション

MGI marker

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

• fascin actin-bundling protein 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2443337

遺伝子型

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

• Fscn2<tm1Sykk>/Fscn2<tm1Sykk>

アレルシンボル

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

• Fscn2<tm1Sykk>

遺伝的背景

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

• involves: 129S4/SvJae * C57BL/6

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

• Shunji. Yokokura, et.al., Targeted disruption of FSCN2 gene induces retinopathy in mice., Investigative ophthalmology & visual science, 2005, 46
  http://rdf.ncbi.nlm.nih.gov/pubmed/16043865