abnormal bone ossification_Sqstm1<tm1.1Sral>/Sqstm1<tm1.1Sral>

http://metadb.riken.jp/0008271I129Sv129P2OlaHsdC57BL6Sqstm1tm11SralSqstm1tm11SralSqstm1tm11Sral

abnormal bone ossification_Sqstm1<tm1.1Sral>/Sqstm1<tm1.1Sral>

表現型アノテーション

MGI marker

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

• sequestosome 1
  http://metadb.riken.jp/db/mgi_rdf/MGI:107931

遺伝子型

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

• Sqstm1<tm1.1Sral>/Sqstm1<tm1.1Sral>

アレルシンボル

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

• Sqstm1<tm1.1Sral>

遺伝的背景

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

• involves: 129/Sv * 129P2/OlaHsd * C57BL/6

MP annotation

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

• abnormal bone ossification
  http://purl.obolibrary.org/obo/MP_0008271

文献

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

• Anna. Daroszewska, et.al., A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice., Human molecular genetics, 2011, 20
  http://rdf.ncbi.nlm.nih.gov/pubmed/21515589