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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Fxyd2 and renal hypomagnesemia 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Meij IC, etal., Nat Genet. 2000 Nov;26(3):265-6.
  • The annotation has been inferred from sequence orthology with FXYD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Meij IC, etal., Nat Genet. 2000 Nov;26(3):265-6.
  • 2 RGD objects have been annotated to renal hypomagnesemia 2  (DOID:0060885)
  • 18 papers in RGD have been used to annotate Fxyd2
  • Curation Notes: DNA:missense mutation:cds:p.G41R (human)


    • An association has been curated linking Fxyd2 and renal hypomagnesemia 2 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 FXYD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to renal hypomagnesemia 2  (DOID:0060885)
  • 18 papers in RGD have been used to annotate Fxyd2


    • An association has been curated linking Fxyd2 and renal hypomagnesemia 2 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FXYD2 (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to renal hypomagnesemia 2  (DOID:0060885)
  • 18 papers in RGD have been used to annotate Fxyd2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Fxyd2 and renal hypomagnesemia 2 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 FXYD2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to renal hypomagnesemia 2  (DOID:0060885)
  • 18 papers in RGD have been used to annotate Fxyd2
  • Curation Notes: ClinVar Annotator: match by term: FXYD2-related condition | ClinVar Annotator: match by term: Renal Hypomagnesemia, Dominant | ClinVar Annotator: match by term: Renal hypomagnesemia 2
  • Original References(s): PMID:11062458 PMID:11929868 PMID:12763860 PMID:16199547 PMID:17576681 PMID:25741868 PMID:25765846 PMID:28492532 PMID:3298795 PMID:9536098


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