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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Padiath QS, etal., Nat Genet. 2006 Oct;38(10):1114-23. Epub 2006 Sep 3.
  • The annotation has been inferred from sequence orthology with LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Padiath QS, etal., Nat Genet. 2006 Oct;38(10):1114-23. Epub 2006 Sep 3.
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1
  • Curation Notes: DNA:duplication:cds (human)


  • An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy 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 LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, Adult-Onset


  • An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy 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 LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, adult-onset, autosomal dominant
  • Original References(s): PMID:16951681, PMID:19151023, PMID:21225301, PMID:21909802, PMID:23649844


  • An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy 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 LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1


  • An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy 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 LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, Adult-Onset
  • Original References(s): PMID:28492532


  • An association has been curated linking Lmnb1 and adult-onset autosomal dominant demyelinating leukodystrophy 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 LMNB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to adult-onset autosomal dominant demyelinating leukodystrophy  (DOID:0060785)
  • 21 papers in CRRD have been used to annotate Lmnb1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, adult-onset, autosomal dominant
  • Original References(s): PMID:25741868


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