renal hypoplasia_Arhgap35<m1Bchd>/Arhgap35<tm1Jset>

http://metadb.riken.jp/0003446I129S2SvPasC3HHeNCrlC57BL6JArhgap35m1BchdArhgap35tm1JsetArhgap35tm1JsetArhgap35m1Bchd

renal hypoplasia_Arhgap35<m1Bchd>/Arhgap35<tm1Jset>

表現型アノテーション

MGI marker

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

• Rho GTPase activating protein 35
  http://metadb.riken.jp/db/mgi_rdf/MGI:1929494

遺伝子型

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

• Arhgap35<m1Bchd>/Arhgap35<tm1Jset>

アレルシンボル

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

• Arhgap35<tm1Jset>|Arhgap35<m1Bchd>

遺伝的背景

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

• involves: 129S2/SvPas * C3H/HeNCrl * C57BL/6J

MP annotation

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

• renal hypoplasia
  http://purl.obolibrary.org/obo/MP_0003446

文献

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

• Katherine. Stewart, et.al., A Point Mutation in p190A RhoGAP Affects Ciliogenesis and Leads to Glomerulocystic Kidney Defects., PLoS genetics, 2016, 12
  http://rdf.ncbi.nlm.nih.gov/pubmed/26859289