no abnormal phenotype detected_Pik3r4<tm1.1Mpnd>/Pik3r4<tm1.1Mpnd>

http://metadb.riken.jp/0002169I129S2SvPasC57BL6NPik3r4tm11MpndPik3r4tm11MpndPik3r4tm11Mpnd

no abnormal phenotype detected_Pik3r4<tm1.1Mpnd>/Pik3r4<tm1.1Mpnd>

表現型アノテーション

MGI marker

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

• phosphoinositide-3-kinase regulatory subunit 4
  http://metadb.riken.jp/db/mgi_rdf/MGI:1922919

遺伝子型

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

• Pik3r4<tm1.1Mpnd>/Pik3r4<tm1.1Mpnd>

アレルシンボル

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

• Pik3r4<tm1.1Mpnd>

遺伝的背景

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

• involves: 129S2/SvPas * C57BL/6N

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

• Ivan. Nemazanyy, et.al., Defects of Vps15 in skeletal muscles lead to autophagic vacuolar myopathy and lysosomal disease., EMBO molecular medicine, 2013, 5
  http://rdf.ncbi.nlm.nih.gov/pubmed/23630012