no abnormal phenotype detected_Arhgap19<Gt(YHD020)Byg>/Arhgap19<Gt(YHD020)Byg>

http://metadb.riken.jp/0002169EI129P2OlaHsdBALBcCrlorI129P2OlaHsdFVBNArhgap19GtYHD020BygArhgap19GtYHD020BygArhgap19GtYHD020Byg

no abnormal phenotype detected_Arhgap19<Gt(YHD020)Byg>/Arhgap19<Gt(YHD020)Byg>

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 19
  http://metadb.riken.jp/db/mgi_rdf/MGI:1918335

遺伝子型

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

• Arhgap19<Gt(YHD020)Byg>/Arhgap19<Gt(YHD020)Byg>

アレルシンボル

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

• Arhgap19<Gt(YHD020)Byg>

遺伝的背景

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

• either: (involves: 129P2/OlaHsd * BALB/cCrl) or (involves: 129P2/OlaHsd * FVB/N)

MP annotation

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

• no abnormal phenotype detected
  http://purl.obolibrary.org/obo/MP_0002169

文献

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

• Megan K. Kooistra, et.al., Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes., Physiological genomics, 2012, 44
  http://rdf.ncbi.nlm.nih.gov/pubmed/22045912