retinal spots_Ap1g1<fgt>/Ap1g1<fgt>

http://metadb.riken.jp/0012671C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt

retinal spots_Ap1g1<fgt>/Ap1g1<fgt>

表現型アノテーション

MGI marker

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

• adaptor protein complex AP-1, gamma 1 subunit
  http://metadb.riken.jp/db/mgi_rdf/MGI:101919

遺伝子型

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

• Ap1g1<fgt>/Ap1g1<fgt>

アレルシンボル

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

• Ap1g1<fgt>

遺伝的背景

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

• C57BL/6-Ap1g1<fgt>/KjnBoc

MP annotation

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

• retinal spots
  http://purl.obolibrary.org/obo/MP_0012671

文献

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

• Kenneth R. Johnson, et.al., A hypomorphic mutation of the gamma-1 adaptin gene (Ap1g1) causes inner ear, retina, thyroid, and testes abnormalities in mice., Mammalian genome : official journal of the International Mammalian Genome Society, 2016, 27
  http://rdf.ncbi.nlm.nih.gov/pubmed/27090238