abnormal amniotic fluid composition_Slc5a3<tm1Gtb>/Slc5a3<tm1Gtb>

http://metadb.riken.jp/0012172I129X1SvJSlc5a3tm1GtbSlc5a3tm1GtbSlc5a3tm1Gtb

abnormal amniotic fluid composition_Slc5a3<tm1Gtb>/Slc5a3<tm1Gtb>

表現型アノテーション

MGI marker

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

• solute carrier family 5 (inositol transporters), member 3
  http://metadb.riken.jp/db/mgi_rdf/MGI:1858226

遺伝子型

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

• Slc5a3<tm1Gtb>/Slc5a3<tm1Gtb>

アレルシンボル

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

• Slc5a3<tm1Gtb>

遺伝的背景

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

• involves: 129X1/SvJ

MP annotation

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

• abnormal amniotic fluid composition
  http://purl.obolibrary.org/obo/MP_0012172

文献

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

• Gerard T. Berry, et.al., Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea., The Journal of biological chemistry, 2003, 278
  http://rdf.ncbi.nlm.nih.gov/pubmed/12582158