hypopigmentation_Ap3b1<pe-rim2>/Ap3b1<pe-rim2>

http://metadb.riken.jp/0005408IB10AR201C57BL10SlcAp3b1perim2Ap3b1perim2Ap3b1perim2

hypopigmentation_Ap3b1<pe-rim2>/Ap3b1<pe-rim2>

表現型アノテーション

MGI marker

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

• adaptor-related protein complex 3, beta 1 subunit
  http://metadb.riken.jp/db/mgi_rdf/MGI:1333879

遺伝子型

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

• Ap3b1<pe-rim2>/Ap3b1<pe-rim2>

アレルシンボル

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

• Ap3b1<pe-rim2>

遺伝的背景

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

• involves: B10.A(R201) * C57BL/10Slc

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

• T. Sagai, et.al., rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping., Mammalian genome : official journal of the International Mammalian Genome Society, 1998, 9
  http://rdf.ncbi.nlm.nih.gov/pubmed/9434937