abnormal electroretinogram waveform feature_Crx<tm2.1Smgc>/Crx<tm2.1Smgc>

http://metadb.riken.jp/0012029B6129X1CBACrxtm21SmgcCrxtm21SmgcCrxtm21SmgcCrxtm21Smgc

abnormal electroretinogram waveform feature_Crx<tm2.1Smgc>/Crx<tm2.1Smgc>

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<tm2.1Smgc>/Crx<tm2.1Smgc>

アレルシンボル

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

• Crx<tm2.1Smgc>

遺伝的背景

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

• B6.129X1(CBA)-Crx<tm2.1Smgc>

MP annotation

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

• abnormal electroretinogram waveform feature
  http://purl.obolibrary.org/obo/MP_0012029

文献

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

• Nicholas M. Tran, et.al., Mechanistically distinct mouse models for CRX-associated retinopathy., PLoS genetics, 2014, 10
  http://rdf.ncbi.nlm.nih.gov/pubmed/24516401