hypopigmentation_Tg(Venus/SOX10*)55Kein/0

http://metadb.riken.jp/0005408IC3HHeC57BL6TgVenusSOX1055Kein0TgVenusSOX1055Kein

hypopigmentation_Tg(Venus/SOX10*)55Kein/0

表現型アノテーション

MGI marker

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

• transgene insertion 55, Ken Inoue
  http://metadb.riken.jp/db/mgi_rdf/MGI:5806869

遺伝子型

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

• Tg(Venus/SOX10*)55Kein/0

アレルシンボル

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

• Tg(Venus/SOX10*)55Kein

遺伝的背景

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

• involves: C3H/He * C57BL/6

MP annotation

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

• hypopigmentation
  http://purl.obolibrary.org/obo/MP_0005408

文献

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

• Yukiko. Ito, et.al., Additive dominant effect of a SOX10 mutation underlies a complex phenotype of PCWH., Neurobiology of disease, 2015, 80
  http://rdf.ncbi.nlm.nih.gov/pubmed/25959061