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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by OMIM:609628
  • Original References(s): PMID:17330256


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by OMIM:609628


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by OMIM:609628
  • Original References(s): PMID:11795677 PMID:15994876


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by OMIM:609628
  • Original References(s): PMID:10969284 PMID:15994876 PMID:2809904


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:15994876 PMID:23087183 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:26386126 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:15994876 PMID:16199547 PMID:23087183 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:16950137 PMID:19369868 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:20032092 PMID:20645851 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:18409191 PMID:20032092 PMID:20645851 PMID:28492532


  • An association has been curated linking Lpin2 and Majeed Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with LPIN2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Majeed Syndrome  (DOID:9005523)
  • 5 papers in RGD have been used to annotate Lpin2
  • Curation Notes: ClinVar Annotator: match by term: Majeed syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


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