no abnormal phenotype detected_Sidt2<tm1Hzha>/Sidt2<tm1Hzha>

http://metadb.riken.jp/0002169I129S6SvEvTacC57BL6JSidt2tm1HzhaSidt2tm1HzhaSidt2tm1Hzha

no abnormal phenotype detected_Sidt2<tm1Hzha>/Sidt2<tm1Hzha>

表現型アノテーション

MGI marker

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

• SID1 transmembrane family, member 2
  http://metadb.riken.jp/db/mgi_rdf/MGI:2446134

遺伝子型

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

• Sidt2<tm1Hzha>/Sidt2<tm1Hzha>

アレルシンボル

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

• Sidt2<tm1Hzha>

遺伝的背景

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

• involves: 129S6/SvEvTac * C57BL/6J

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

• Jialin. Gao, et.al., Impaired glucose tolerance in a mouse model of sidt2 deficiency., PloS one, 2013, 8
  http://rdf.ncbi.nlm.nih.gov/pubmed/23776622