abnormal cranium morphology_Ift80<Gt(AN0245)Wtsi>/Ift80<Gt(AN0245)Wtsi>

http://metadb.riken.jp/0000438I129P2OlaHsdIft80GtAN0245WtsiIft80GtAN0245WtsiIft80GtAN0245Wtsi

abnormal cranium morphology_Ift80<Gt(AN0245)Wtsi>/Ift80<Gt(AN0245)Wtsi>

表現型アノテーション

MGI marker

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

• intraflagellar transport 80
  http://metadb.riken.jp/db/mgi_rdf/MGI:1915509

遺伝子型

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

• Ift80<Gt(AN0245)Wtsi>/Ift80<Gt(AN0245)Wtsi>

アレルシンボル

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

• Ift80<Gt(AN0245)Wtsi>

遺伝的背景

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

• involves: 129P2/OlaHsd

MP annotation

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

• abnormal cranium morphology
  http://purl.obolibrary.org/obo/MP_0000438

文献

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

• Suzanne. Rix, et.al., An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21227999