hypopigmentation_mwfh<C3HeB/FeJLe>/mwfh<C3HeB/FeJLe>,Sox10<Dom>/?

http://metadb.riken.jp/0005408IC3HeBFeJLeC57BL6JLemwfhC3HeBFeJLemwfhC3HeBFeJLeSox10DomSox10DommwfhC3HeBFeJLe

hypopigmentation_mwfh<C3HeB/FeJLe>/mwfh<C3HeB/FeJLe>,Sox10<Dom>/?

表現型アノテーション

MGI marker

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

• modifier of white forlock hypopigmentation
  http://metadb.riken.jp/db/mgi_rdf/MGI:1344358
• SRY (sex determining region Y)-box 10
  http://metadb.riken.jp/db/mgi_rdf/MGI:98358

遺伝子型

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

• mwfh<C3HeB/FeJLe>/mwfh<C3HeB/FeJLe>,Sox10<Dom>/?

アレルシンボル

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

• Sox10<Dom>|mwfh<C3HeB/FeJLe>

遺伝的背景

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

• involves: C3HeB/FeJLe * C57BL/6JLe

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

• E M. Southard-Smith, et.al., The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome., Genome research, 1999, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/10077527