abnormal vision_Lrit3<tm1Lex>/Lrit3<tm1Lex>

http://metadb.riken.jp/0002090I129S5SvEvBrdC57BL6Lrit3tm1LexLrit3tm1LexLrit3tm1Lex

abnormal vision_Lrit3<tm1Lex>/Lrit3<tm1Lex>

表現型アノテーション

MGI marker

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

• leucine-rich repeat, immunoglobulin-like and transmembrane domains 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:2685267

遺伝子型

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

• Lrit3<tm1Lex>/Lrit3<tm1Lex>

アレルシンボル

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

• Lrit3<tm1Lex>

遺伝的背景

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

• involves: 129S5/SvEvBrd * C57BL/6

MP annotation

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

• abnormal vision
  http://purl.obolibrary.org/obo/MP_0002090

文献

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

• Marion. Neuillé, et.al., Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB)., PloS one, 2014, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/24598786