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GENE - TERM ANNOTATION REPORT

27 Annotations Found.

An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11639520 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi myopathy 3
  • Original References(s): PMID:23606453 PMID:23607914 PMID:25741868 PMID:25891276 PMID:28492532 PMID:30564623 PMID:30919934 PMID:31350120 PMID:32112655


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Bolduc V, etal., Am J Hum Genet. 2010 Feb 12;86(2):213-21. doi: 10.1016/j.ajhg.2009.12.013. Epub 2010 Jan 21.
  • 5 additional annotations were made from Bolduc V, etal., Am J Hum Genet. 2010 Feb 12;86(2):213-21. doi: 10.1016/j.ajhg.2009.12.013. Epub 2010 Jan 21.
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: DNA:duplication, missense mutation:exon:c.191dupA, p.R758C (c.2272C>T) (human)


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11633243 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi myopathy 3
  • Original References(s): PMID:21186264 PMID:23606453 PMID:25741868 PMID:25891276 PMID:27862037 PMID:28492532 PMID:30919934


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11633914 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:21186264 PMID:23606453 PMID:23663589 PMID:25741868 PMID:25891276 PMID:28492532 PMID:30919934


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11580230 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:21186264 PMID:22194990 PMID:22402862 PMID:22742934 PMID:23606453 PMID:25741868 PMID:25891276 PMID:28492532 PMID:30919934 PMID:34008892


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8658979 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:23041008 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11642727 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:23606453 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:13211795 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:23530687 PMID:25741868 PMID:25864073 PMID:28492532 PMID:33963534


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11089249 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:25891276 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8643594 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:10048257 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:22980763 PMID:23041008 PMID:23606453 PMID:25741868 PMID:25891276 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8696313 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:21186264 PMID:22742934 PMID:23041008 PMID:23606453 PMID:23663589 PMID:23670307 PMID:25046369 PMID:25741868 PMID:25891276 PMID:26467025 PMID:26838040 PMID:28492532 PMID:28888072 PMID:30919934


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8604232 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:22402862 PMID:23193613


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11643893 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:25741868 PMID:26886200 PMID:27911336 PMID:28492532 PMID:30564623 PMID:31395899 PMID:32112655


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:10048762 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:22336395 PMID:22499103 PMID:23041008 PMID:23670307 PMID:25741868 PMID:25741916 PMID:25864073 PMID:25891276 PMID:26467025 PMID:27671536 PMID:27854218 PMID:28492532 PMID:32528171 PMID:32925086 PMID:33496727 PMID:36913258


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8595648 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:17132147 PMID:20096397 PMID:20692837 PMID:21186264 PMID:21739273 PMID:22402862 PMID:22980763 PMID:23193613 PMID:23670307 PMID:24033266 PMID:24803842 PMID:25135358 PMID:25741868 PMID:25891276 PMID:26467025 PMID:27911336 PMID:28489263 PMID:28492532 PMID:30564623 PMID:31341644 PMID:31353849 PMID:31395899 PMID:31589614 PMID:34008892


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11580884 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi myopathy 3
  • Original References(s): PMID:23607914 PMID:23663589 PMID:25741868 PMID:25891276 PMID:26467025 PMID:28492532 PMID:29431110 PMID:30919934 PMID:31350120 PMID:31353849 PMID:31561939 PMID:32528171 PMID:34008892


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8595647 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi myopathy 3
  • Original References(s): PMID:20096397 PMID:22402862 PMID:22980763 PMID:23041008 PMID:23193613 PMID:23606453 PMID:23663589 PMID:23670307 PMID:24033266 PMID:25741868 PMID:25891276 PMID:26467025 PMID:26810512 PMID:28176803 PMID:28492532 PMID:30919934 PMID:31353849 PMID:31931849 PMID:32367299 PMID:32403337 PMID:32528171


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8595646 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:20096397 PMID:21186264 PMID:21739273 PMID:21820307 PMID:22194990 PMID:22336395 PMID:22402862 PMID:22499103 PMID:22742934 PMID:22980763 PMID:23041008 PMID:23606453 PMID:23607914 PMID:23757202 PMID:24022920 PMID:24232312 PMID:24843231 PMID:25741868 PMID:25891276 PMID:26467025 PMID:26886200 PMID:27708273 PMID:27911336 PMID:28187523 PMID:28492532 PMID:30919934 PMID:9673985


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:38598767 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:21186264 PMID:23606453 PMID:25891276 PMID:28492532 PMID:30919934 PMID:32528171


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11544497|RGD:8658980 (Homo sapiens) & RGD:11544497|RGD:8658980 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:25741868 PMID:25891276 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:8643591|RGD:8643597 (Homo sapiens) & RGD:8643591|RGD:8643597 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens) & RGD:10048258|RGD:11640188|RGD:13520226|RGD:150334355|RGD:152063795|RGD:8643588|RGD:8643590|RGD:8643596|RGD:8696306 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11549939|RGD:8696310 (Homo sapiens) & RGD:11549939|RGD:8696310 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ANO5 and Miyoshi muscular dystrophy 3 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:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens) & RGD:11548055|RGD:11549128|RGD:11598738|RGD:11599207|RGD:11604699|RGD:11607615|RGD:11617829|RGD:11618918|RGD:11620351|RGD:11621184|RGD:11621291|RGD:11658712|RGD:126746332|RGD:13704896|RGD:14708717|RGD:150434755|RGD:21072022|RGD:28900457|RGD:401720967|RGD:8696304|RGD:8696307|RGD:8696317 (Homo sapiens)
  • 2 RGD objects have been annotated to Miyoshi muscular dystrophy 3  (DOID:0070201)
  • 11 papers in RGD have been used to annotate ANO5
  • Curation Notes: ClinVar Annotator: match by term: Miyoshi muscular dystrophy 3
  • Original References(s): PMID:25741868


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