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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking LOC105376196 and primary hypoalphalipoproteinemia 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:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens) & RGD:11600068|RGD:11607227|RGD:11608264|RGD:11610560|RGD:11610906|RGD:11644351|RGD:11648128|RGD:11652565|RGD:11653187|RGD:11656958|RGD:28874994|RGD:28874997|RGD:28879740|RGD:28888246|RGD:28888250 (Homo sapiens)
  • 8 RGD objects have been annotated to primary hypoalphalipoproteinemia 1  (DOID:0080957)
  • 0 papers in RGD have been used to annotate LOC105376196
  • Curation Notes: ClinVar Annotator: match by term: Familial High Density Lipoprotein Deficiency | ClinVar Annotator: match by term: Hypoalphalipoproteinemia, primary, 1


    • An association has been curated linking LOC105376196 and primary hypoalphalipoproteinemia 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:11666323 (Homo sapiens)
  • 8 RGD objects have been annotated to primary hypoalphalipoproteinemia 1  (DOID:0080957)
  • 0 papers in RGD have been used to annotate LOC105376196
  • Curation Notes: ClinVar Annotator: match by term: Familial High Density Lipoprotein Deficiency
  • Original References(s): PMID:11940086 PMID:25741868


    • An association has been curated linking LOC105376196 and primary hypoalphalipoproteinemia 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:11606519 (Homo sapiens)
  • 8 RGD objects have been annotated to primary hypoalphalipoproteinemia 1  (DOID:0080957)
  • 0 papers in RGD have been used to annotate LOC105376196
  • Curation Notes: ClinVar Annotator: match by term: Familial High Density Lipoprotein Deficiency
  • Original References(s): PMID:11940086 PMID:20595220 PMID:25741868


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