abnormal retinal pigment epithelium morphology_Adam9<tm1Bbl>/Adam9<tm1Bbl>

http://metadb.riken.jp/0005201I129SvAdam9tm1BblAdam9tm1BblAdam9tm1Bbl

abnormal retinal pigment epithelium morphology_Adam9<tm1Bbl>/Adam9<tm1Bbl>

表現型アノテーション

MGI marker

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

• a disintegrin and metallopeptidase domain 9 (meltrin gamma)
  http://metadb.riken.jp/db/mgi_rdf/MGI:105376

遺伝子型

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

• Adam9<tm1Bbl>/Adam9<tm1Bbl>

アレルシンボル

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

• Adam9<tm1Bbl>

遺伝的背景

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

• involves: 129/Sv

MP annotation

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

• abnormal retinal pigment epithelium morphology
  http://purl.obolibrary.org/obo/MP_0005201

文献

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

• David A. Parry, et.al., Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice., American journal of human genetics, 2009, 84
  http://rdf.ncbi.nlm.nih.gov/pubmed/19409519