retinal pigment epithelium atrophy_Nmnat1<imh>/Nmnat1<imh>

http://metadb.riken.jp/0005548B6JCC3HNmnat1imhNmnat1imhNmnat1imhNmnat1imh

retinal pigment epithelium atrophy_Nmnat1<imh>/Nmnat1<imh>

表現型アノテーション

MGI marker

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

• nicotinamide nucleotide adenylyltransferase 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1913704

遺伝子型

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

• Nmnat1<imh>/Nmnat1<imh>

アレルシンボル

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

• Nmnat1<imh>

遺伝的背景

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

• B6J.C(C3H)-Nmnat1<imh>

MP annotation

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

• retinal pigment epithelium atrophy
  http://purl.obolibrary.org/obo/MP_0005548

文献

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

• Scott H. Greenwald, et.al., Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease., The American journal of pathology, 2016, 186
  http://rdf.ncbi.nlm.nih.gov/pubmed/27207593