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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking MIR2392 and Uniparental Disomy, Paternal, Chromosome 14 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:9687353 (Homo sapiens)
  • 104 CRRD objects have been annotated to Uniparental Disomy, Paternal, Chromosome 14  (DOID:9005066)
  • 1 papers in CRRD have been used to annotate MIR2392
  • Curation Notes: ClinVar Annotator: match by term: Uniparental disomy, paternal, chromosome 14
  • Original References(s): PMID:18176563

  • This annotation was curated on 2020-02-11 06:40:46.0 by CRRD . For more information contact us

    An association has been curated linking MIR2392 and Uniparental Disomy, Paternal, Chromosome 14 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:9687354 (Homo sapiens)
  • 104 CRRD objects have been annotated to Uniparental Disomy, Paternal, Chromosome 14  (DOID:9005066)
  • 1 papers in CRRD have been used to annotate MIR2392
  • Curation Notes: ClinVar Annotator: match by term: Uniparental disomy, paternal, chromosome 14
  • Original References(s): PMID:18176563

  • This annotation was curated on 2020-02-11 06:40:48.0 by CRRD . For more information contact us

    An association has been curated linking MIR2392 and Uniparental Disomy, Paternal, Chromosome 14 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:9687352 (Homo sapiens)
  • 104 CRRD objects have been annotated to Uniparental Disomy, Paternal, Chromosome 14  (DOID:9005066)
  • 1 papers in CRRD have been used to annotate MIR2392
  • Curation Notes: ClinVar Annotator: match by term: Uniparental disomy, paternal, chromosome 14
  • Original References(s): PMID:18176563

  • This annotation was curated on 2020-02-11 06:40:45.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.