S L. Bullock, et.al., Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase., Genes & development, 1998, 12

http://rdf.ncbi.nlm.nih.gov/pubmed/9637690

S L. Bullock, et.al., Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase., Genes & development, 1998, 12

http://rdf.ncbi.nlm.nih.gov/pubmed/

トランスクリプトームデータ

http://rdf.ncbi.nlm.nih.gov/pubmed/

• CD01202
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD01202

allele

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

• Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/db/mgi_rdf/MGI:1934916

表現型アノテーション

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

• abnormal eye development_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0001286I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• polydactyly_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0000562I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• abnormal bone mineralization_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0002896I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• iris coloboma_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0010714I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• cataract_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0001304I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• perinatal lethality, complete penetrance_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0011089I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• cleft secondary palate_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0009890I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• abnormal retinal pigment epithelium morphology_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0005201I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• abnormal sternum ossification_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0008277I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• abnormal kidney development_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0000527I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• abnormal ureteric bud morphology_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0006032I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• impaired branching involved in ureteric bud morphogenesis_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0004936I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• cervical vertebral fusion_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0004620I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr
• absent kidney_Hs2st1<Gt(pGT1.8TM)ST125Nimr>/Hs2st1<Gt(pGT1.8TM)ST125Nimr>
  http://metadb.riken.jp/0000520I129P2OlaHsdC57BL6Hs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125NimrHs2st1GtpGT18TMST125Nimr