no abnormal phenotype detected_Bbs2<tm1Vcs>/Bbs2<+>,Bbs4<tm1Vcs>/Bbs4<+>

http://metadb.riken.jp/0002169EI129S1Sv129X1SvJorI129S1Sv129X1SvJC57BL6JBbs2tm1VcsBbs2Bbs4tm1VcsBbs4Bbs2Bbs4tm1VcsBbs2tm1VcsBbs4

no abnormal phenotype detected_Bbs2<tm1Vcs>/Bbs2<+>,Bbs4<tm1Vcs>/Bbs4<+>

表現型アノテーション

MGI marker

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

• Bardet-Biedl syndrome 4 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:2143311
• Bardet-Biedl syndrome 2 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:2135267

遺伝子型

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

• Bbs2<tm1Vcs>/Bbs2<+>,Bbs4<tm1Vcs>/Bbs4<+>

アレルシンボル

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

• Bbs2<+>|Bbs4<tm1Vcs>|Bbs2<tm1Vcs>|Bbs4<+>

遺伝的背景

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

• either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Darryl Y. Nishimura, et.al., Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin., Proceedings of the National Academy of Sciences of the United States of America, 2004, 101
  http://rdf.ncbi.nlm.nih.gov/pubmed/15539463