glomerulosclerosis_Myh9<tm1.1Dash>/Myh9<+>

http://metadb.riken.jp/0005264I129S2SvPasC57BL6C57BL6JCBAMyh9tm11DashMyh9Myh9Myh9tm11Dash

glomerulosclerosis_Myh9<tm1.1Dash>/Myh9<+>

表現型アノテーション

MGI marker

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

• myosin, heavy polypeptide 9, non-muscle
  http://metadb.riken.jp/db/mgi_rdf/MGI:107717

遺伝子型

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

• Myh9<tm1.1Dash>/Myh9<+>

アレルシンボル

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

• Myh9<+>|Myh9<tm1.1Dash>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA

MP annotation

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

• glomerulosclerosis
  http://purl.obolibrary.org/obo/MP_0005264

文献

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

• Nobuaki. Suzuki, et.al., Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability., PloS one, 2013, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/23976996