abnormal limb development_Bbs7<tm1Vcs>/Bbs7<tm1Vcs>,Ift88<Tg737Rpw>/Ift88<Tg737Rpw>

http://metadb.riken.jp/0006279IFVBNBbs7tm1VcsBbs7tm1VcsIft88Tg737RpwIft88Tg737RpwIft88Tg737RpwBbs7tm1Vcs

abnormal limb development_Bbs7<tm1Vcs>/Bbs7<tm1Vcs>,Ift88<Tg737Rpw>/Ift88<Tg737Rpw>

表現型アノテーション

MGI marker

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

• Bardet-Biedl syndrome 7 (human)
  http://metadb.riken.jp/db/mgi_rdf/MGI:1918742
• intraflagellar transport 88
  http://metadb.riken.jp/db/mgi_rdf/MGI:98715

遺伝子型

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

• Bbs7<tm1Vcs>/Bbs7<tm1Vcs>,Ift88<Tg737Rpw>/Ift88<Tg737Rpw>

アレルシンボル

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

• Ift88<Tg737Rpw>|Bbs7<tm1Vcs>

遺伝的背景

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

• involves: FVB/N

MP annotation

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

• abnormal limb development
  http://purl.obolibrary.org/obo/MP_0006279

文献

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

• Qihong. Zhang, et.al., BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes., Human molecular genetics, 2012, 21
  http://rdf.ncbi.nlm.nih.gov/pubmed/22228099