abnormal rod electrophysiology_Crx<Rip>/Crx<+>

http://metadb.riken.jp/0004021C57BL6JCrxRipCrxRipCrxCrxCrxRip

abnormal rod electrophysiology_Crx<Rip>/Crx<+>

表現型アノテーション

MGI marker

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

• cone-rod homeobox
  http://metadb.riken.jp/db/mgi_rdf/MGI:1194883

遺伝子型

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

• Crx<Rip>/Crx<+>

アレルシンボル

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

• Crx<+>|Crx<Rip>

遺伝的背景

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

• C57BL/6J-Crx<Rip>

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

• Jerome E. Roger, et.al., OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness., The Journal of clinical investigation, 2014, 124
  http://rdf.ncbi.nlm.nih.gov/pubmed/24382353