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

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

pubmed

allele

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

• Ap1g1<fgt>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5755140

表現型アノテーション

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

• circling_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001394IC3HeBFeJC57BL6JAp1g1fgtAp1g1fgtAp1g1fgt
• choroidal neovascularization_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0005546C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• organ of Corti degeneration_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0000043C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• asthenozoospermia_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0002675C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• oligozoospermia_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0002687C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• cochlear outer hair cell degeneration_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004404C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• impaired swimming_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001522C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• retinal degeneration_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001326C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• reduced male fertility_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001922C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• head tossing_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0005307IC3HeBFeJC57BL6JAp1g1fgtAp1g1fgtAp1g1fgt
• decreased body weight_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001262C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• circling_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0001394C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• head tilt_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0005191C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• abnormal thyroid follicular cell morphology_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004697C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• kinked sperm flagellum_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0009237C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• decreased vestibular hair cell number_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004328C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• increased or absent threshold for auditory brainstem response_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0011967C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• decreased male germ cell number_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004901C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• retinal spots_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0012671C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• abnormal thyroid gland morphology_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0000681C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• decreased cochlear outer hair cell number_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004402C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• abnormal thyroid follicle morphology_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004696C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• head tossing_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0005307C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• vestibular hair cell degeneration_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0004324C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt
• decreased circulating thyroxine level_Ap1g1<fgt>/Ap1g1<fgt>
  http://metadb.riken.jp/0005478C57BL6Ap1g1fgtKjnBocAp1g1fgtAp1g1fgtAp1g1fgt

class

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

• Ap1g1<fgt>
  http://metadb.riken.jp/db/mgi_rdf/MGI:5755140