microphthalmia_B9d1<tm1a(EUCOMM)Wtsi>/B9d1<tm1a(EUCOMM)Wtsi>

http://metadb.riken.jp/0001297IC57BL6NCD1B9d1tm1aEUCOMMWtsiB9d1tm1aEUCOMMWtsiB9d1tm1aEUCOMMWtsi

microphthalmia_B9d1<tm1a(EUCOMM)Wtsi>/B9d1<tm1a(EUCOMM)Wtsi>

表現型アノテーション

MGI marker

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

• B9 protein domain 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:1351471

遺伝子型

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

• B9d1<tm1a(EUCOMM)Wtsi>/B9d1<tm1a(EUCOMM)Wtsi>

アレルシンボル

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

• B9d1<tm1a(EUCOMM)Wtsi>

遺伝的背景

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

• involves: C57BL/6N * CD-1

MP annotation

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

• microphthalmia
  http://purl.obolibrary.org/obo/MP_0001297

文献

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

• William E. Dowdle, et.al., Disruption of a ciliary B9 protein complex causes Meckel syndrome., American journal of human genetics, 2011, 89
  http://rdf.ncbi.nlm.nih.gov/pubmed/21763481