retinal degeneration_Cep290<tm1Jgg>/Cep290<tm1Jgg>

http://metadb.riken.jp/0001326I129Cep290tm1JggCep290tm1JggCep290tm1Jgg

retinal degeneration_Cep290<tm1Jgg>/Cep290<tm1Jgg>

表現型アノテーション

MGI marker

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

• centrosomal protein 290
  http://metadb.riken.jp/db/mgi_rdf/MGI:2384917

遺伝子型

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

• Cep290<tm1Jgg>/Cep290<tm1Jgg>

アレルシンボル

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

• Cep290<tm1Jgg>

遺伝的背景

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

• involves: 129

MP annotation

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

• retinal degeneration
  http://purl.obolibrary.org/obo/MP_0001326

文献

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

• Madeline A. Lancaster, et.al., Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome., Nature medicine, 2011, 17
  http://rdf.ncbi.nlm.nih.gov/pubmed/21623382