osteoporosis_Crtap<tm1Brle>/Crtap<tm1Brle>

http://metadb.riken.jp/0000066I129S7SvEvBrdCrtaptm1BrleCrtaptm1BrleCrtaptm1Brle

osteoporosis_Crtap<tm1Brle>/Crtap<tm1Brle>

表現型アノテーション

MGI marker

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

• cartilage associated protein
  http://metadb.riken.jp/db/mgi_rdf/MGI:1891221

遺伝子型

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

• Crtap<tm1Brle>/Crtap<tm1Brle>

アレルシンボル

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

• Crtap<tm1Brle>

遺伝的背景

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

• involves: 129S7/SvEvBrd

MP annotation

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

• osteoporosis
  http://purl.obolibrary.org/obo/MP_0000066

文献

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

• Roy. Morello, et.al., CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta., Cell, 2006, 127
  http://rdf.ncbi.nlm.nih.gov/pubmed/17055431