abnormal coat/hair pigmentation_Kit<W-39H>/Kit<+>

http://metadb.riken.jp/0002075IBALBcCrlC3HHeNCrlKitW39HKitKitW39HKit

abnormal coat/hair pigmentation_Kit<W-39H>/Kit<+>

表現型アノテーション

MGI marker

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

• KIT proto-oncogene receptor tyrosine kinase
  http://metadb.riken.jp/db/mgi_rdf/MGI:96677

遺伝子型

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

• Kit<W-39H>/Kit<+>

アレルシンボル

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

• Kit<W-39H>|Kit<+>

遺伝的背景

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

• involves: BALB/cCrl * C3H/HeNCrl

MP annotation

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

• abnormal coat/hair pigmentation
  http://purl.obolibrary.org/obo/MP_0002075

文献

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

• P M. Nolan, et.al., A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse., Nature genetics, 2000, 25
  http://rdf.ncbi.nlm.nih.gov/pubmed/10932191