abnormal eye electrophysiology_Aipl1<tm1Tili>/Aipl1<tm1Tili>

http://metadb.riken.jp/0005551I129S4SvJaeC57BL6Aipl1tm1TiliAipl1tm1TiliAipl1tm1Tili

abnormal eye electrophysiology_Aipl1<tm1Tili>/Aipl1<tm1Tili>

表現型アノテーション

MGI marker

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

• aryl hydrocarbon receptor-interacting protein-like 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:2148800

遺伝子型

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

• Aipl1<tm1Tili>/Aipl1<tm1Tili>

アレルシンボル

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

• Aipl1<tm1Tili>

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 eye electrophysiology
  http://purl.obolibrary.org/obo/MP_0005551

文献

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

• Xiaoqing. Liu, et.al., AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase., Proceedings of the National Academy of Sciences of the United States of America, 2004, 101
  http://rdf.ncbi.nlm.nih.gov/pubmed/15365173