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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking LOC126806951 and fetal akinesia deformation sequence syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14714966 (Homo sapiens)
  • 78 RGD objects have been annotated to fetal akinesia deformation sequence syndrome 1  (DOID:0111377)
  • 0 papers in RGD have been used to annotate LOC126806951
  • Curation Notes: ClinVar Annotator: match by term: Fetal akinesia deformation sequence 1
  • Original References(s): PMID:16917026 PMID:18165682 PMID:28492532


    • An association has been curated linking LOC126806951 and fetal akinesia deformation sequence syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151751332 (Homo sapiens)
  • 78 RGD objects have been annotated to fetal akinesia deformation sequence syndrome 1  (DOID:0111377)
  • 0 papers in RGD have been used to annotate LOC126806951
  • Curation Notes: ClinVar Annotator: match by term: Fetal akinesia deformation sequence 1
  • Original References(s): PMID:16199547 PMID:16794080 PMID:16917026 PMID:18626973 PMID:19261599 PMID:28492532


    • An association has been curated linking LOC126806951 and fetal akinesia deformation sequence syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens) & RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens) & RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens) & RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens) & RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens) & RGD:11545925|RGD:126755687|RGD:12900537|RGD:14712598|RGD:151866020|RGD:38473098 (Homo sapiens)
  • 78 RGD objects have been annotated to fetal akinesia deformation sequence syndrome 1  (DOID:0111377)
  • 0 papers in RGD have been used to annotate LOC126806951
  • Curation Notes: ClinVar Annotator: match by term: Fetal akinesia deformation sequence 1
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC126806951 and fetal akinesia deformation sequence syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens) & RGD:126754171|RGD:126766035|RGD:127297960|RGD:127330899|RGD:13471966|RGD:13484143|RGD:15119569|RGD:15171877|RGD:151746948|RGD:151749724|RGD:151800669|RGD:151837677|RGD:152037191|RGD:152076036|RGD:156051537|RGD:156312640|RGD:26886775|RGD:401863426|RGD:402514161|RGD:404997155|RGD:405005930|RGD:405028323|RGD:405038918|RGD:405051243|RGD:405056410|RGD:405089960 (Homo sapiens)
  • 78 RGD objects have been annotated to fetal akinesia deformation sequence syndrome 1  (DOID:0111377)
  • 0 papers in RGD have been used to annotate LOC126806951
  • Curation Notes: ClinVar Annotator: match by term: Fetal akinesia deformation sequence 1
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC126806951 and fetal akinesia deformation sequence syndrome 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8556085 (Homo sapiens)
  • 78 RGD objects have been annotated to fetal akinesia deformation sequence syndrome 1  (DOID:0111377)
  • 0 papers in RGD have been used to annotate LOC126806951
  • Curation Notes: ClinVar Annotator: match by term: Fetal akinesia deformation sequence 1
  • Original References(s): PMID:16917026 PMID:17452375 PMID:18567858 PMID:28492532 PMID:29118959


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