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GENE - TERM ANNOTATION REPORT

45 Annotations Found.

An association has been curated linking FAM20C and Raine Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Simpson MA, etal., Am J Hum Genet. 2007 Nov;81(5):906-12. Epub 2007 Sep 14.
  • 5 additional annotations were made from Simpson MA, etal., Am J Hum Genet. 2007 Nov;81(5):906-12. Epub 2007 Sep 14.
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: DNA:deletion, snps, missense mutations:multiple (human)


  • An association has been curated linking FAM20C and Raine Syndrome 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:8568643 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:19250384


  • An association has been curated linking FAM20C and Raine Syndrome 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:11636304 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:8568644 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:19250384


  • An association has been curated linking FAM20C and Raine Syndrome 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:13444450 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome


  • An association has been curated linking FAM20C and Raine Syndrome 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:8595274 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555933 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555929 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:12868469 PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555927 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:14564151 PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555932 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8568646 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:20825432


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555931 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555930 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:17924334


  • An association has been curated linking FAM20C and Raine Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C


  • An association has been curated linking FAM20C and Raine Syndrome 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:12895923 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Raine syndrome
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:150409841 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:150409847 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:150409851 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:10047680 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:10047681 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:150333678 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:127307329 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:150409858 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:11638422 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:38461100 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:127314857 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:152155244 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:27862258


  • An association has been curated linking FAM20C and Raine Syndrome 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:152155243 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:27862258


  • An association has been curated linking FAM20C and Raine Syndrome 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:10047679 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:152059798 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:150438779 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:127312335 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:38476431 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:151802415 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:151348308 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868


  • An association has been curated linking FAM20C and Raine Syndrome 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:156252930 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: FAM20C-related condition
  • Original References(s): PMID:17924334 PMID:22582013 PMID:25741868 PMID:28492532 PMID:32299476


  • An association has been curated linking FAM20C and Raine Syndrome 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:152131028 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:127296207 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:127312467 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:15111904 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:126733362 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:8568645 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:19250384 PMID:28492532


  • An association has been curated linking FAM20C and Raine Syndrome 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:8555928 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:17924334 PMID:2020859 PMID:25026495 PMID:28492532 PMID:32337609


  • An association has been curated linking FAM20C and Raine Syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking FAM20C and Raine Syndrome 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:401924695 (Homo sapiens)
  • 1 RGD objects have been annotated to Raine Syndrome  (DOID:9000666)
  • 11 papers in RGD have been used to annotate FAM20C
  • Curation Notes: ClinVar Annotator: match by term: Lethal osteosclerotic bone dysplasia
  • Original References(s): PMID:32093234


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