abnormal retinal photoreceptor layer morphology_Crx<tm1Clc>/Crx<tm1Clc>

http://metadb.riken.jp/0003728I129S6SvEvTacC57BL6JCrxtm1ClcCrxtm1ClcCrxtm1Clc

abnormal retinal photoreceptor layer morphology_Crx<tm1Clc>/Crx<tm1Clc>

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<tm1Clc>/Crx<tm1Clc>

アレルシンボル

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

• Crx<tm1Clc>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6J

MP annotation

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

• abnormal retinal photoreceptor layer morphology
  http://purl.obolibrary.org/obo/MP_0003728

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