abnormal retinal photoreceptor morphology_Fam161a<Gt(462E7)Cmhd>/Fam161a<Gt(462E7)Cmhd>

http://metadb.riken.jp/0001004I129S1Sv129X1SvJC57BL6JFam161aGt462E7CmhdFam161aGt462E7CmhdFam161aGt462E7Cmhd

abnormal retinal photoreceptor morphology_Fam161a<Gt(462E7)Cmhd>/Fam161a<Gt(462E7)Cmhd>

表現型アノテーション

MGI marker

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

• family with sequence similarity 161, member A
  http://metadb.riken.jp/db/mgi_rdf/MGI:1921123

遺伝子型

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

• Fam161a<Gt(462E7)Cmhd>/Fam161a<Gt(462E7)Cmhd>

アレルシンボル

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

• Fam161a<Gt(462E7)Cmhd>

遺伝的背景

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

• involves: 129S1/Sv * 129X1/SvJ * C57BL/6J

MP annotation

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

• abnormal retinal photoreceptor morphology
  http://purl.obolibrary.org/obo/MP_0001004

文献

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

• Marcus. Karlstetter, et.al., Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration., Human molecular genetics, 2014, 23
  http://rdf.ncbi.nlm.nih.gov/pubmed/24833722