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GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by OMIM:607143
  • Original References(s): PMID:11983712 PMID:12736397


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by OMIM:607143
  • Original References(s): PMID:12217961


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by OMIM:607143
  • Original References(s): PMID:17506107


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by OMIM:607143
  • Original References(s): PMID:12093361


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by OMIM:607143
  • Original References(s): PMID:25019053


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: ALG12-congenital disorder of glycosylation
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: ALG12-congenital disorder of glycosylation
  • Original References(s): PMID:25019053 PMID:25741868 PMID:31481313


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: ALG12-congenital disorder of glycosylation
  • Original References(s): PMID:19862844 PMID:28492532


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1G
  • Original References(s): PMID:28492532


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1G
  • Original References(s): PMID:12217961 PMID:17506107 PMID:25326635 PMID:25741868


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1G
  • Original References(s): PMID:25326635 PMID:25741868


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1G
  • Original References(s): PMID:25741868


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1G


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: ALG12-congenital disorder of glycosylation
  • Original References(s): PMID:15639192 PMID:28492532


    • An association has been curated linking Alg12 and congenital disorder of glycosylation Ig 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 ALG12 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation Ig  (DOID:0080559)
  • 6 papers in RGD have been used to annotate Alg12
  • Curation Notes: ClinVar Annotator: match by term: ALG12-congenital disorder of glycosylation
  • Original References(s): PMID:28492532 PMID:31481313


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