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GENE - TERM ANNOTATION REPORT

23 Annotations Found.

An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595715 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:15064763 PMID:16437557 PMID:16714318 PMID:16835246 PMID:17215403 PMID:17296794 PMID:19889647 PMID:20418531 PMID:21285398 PMID:21508331 PMID:22442078 PMID:24126688 PMID:24604904 PMID:24862862 PMID:24863639 PMID:25025039 PMID:25741868 PMID:26085578 PMID:26382835 PMID:26467025 PMID:26686600 PMID:26801520 PMID:27549087 PMID:27863451 PMID:28492532 PMID:31130284 PMID:31188717 PMID:31832804 PMID:32376792 PMID:33475540 PMID:33841295 PMID:34366782 PMID:35938991


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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 Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595720 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:18316077 PMID:18425620 PMID:18946002 PMID:18957892 PMID:20008656 PMID:21326314 PMID:21531138 PMID:21840889 PMID:22492563 PMID:24088041 PMID:24803844 PMID:24957169 PMID:25025039 PMID:25741868 PMID:26307494 PMID:26382835 PMID:26633542 PMID:26633545 PMID:28492532 PMID:28660751 PMID:31673878


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:11523010 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:23806086 PMID:24088041 PMID:26257172


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:10049260 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16043786 PMID:19889647 PMID:21576112 PMID:25741868 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595721 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16762064 PMID:19889647 PMID:20350294 PMID:21258814 PMID:21519004 PMID:25403865 PMID:25741868 PMID:26143526 PMID:26382835 PMID:26392352 PMID:26467025 PMID:27582484 PMID:28251916 PMID:28492532 PMID:29473246


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:28879200 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:25741868 PMID:26454100


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:10410244 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:25741868 PMID:26686600 PMID:28492532 PMID:29625556 PMID:30340945 PMID:31108397


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595708 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:15064763 PMID:16714318 PMID:17215403 PMID:17296794 PMID:20335458 PMID:21508331 PMID:23806086 PMID:24088041 PMID:24126688 PMID:25614874 PMID:25741868 PMID:26257172 PMID:26467025 PMID:28492532 PMID:29068134 PMID:29341354 PMID:29361379 PMID:29790872 PMID:30649465 PMID:32399692 PMID:33415332 PMID:8406488


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8602309 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16835246 PMID:18458227 PMID:18957892 PMID:21715711 PMID:24819634 PMID:24863639 PMID:25741868 PMID:26114802 PMID:26467025 PMID:28492532 PMID:29625556 PMID:29858556 PMID:31673878 PMID:31701603 PMID:33415332 PMID:33475540


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8691954 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:16762064 PMID:16930284 PMID:20350294 PMID:22494076 PMID:23456260 PMID:24126688 PMID:25741868 PMID:26316991 PMID:26467025 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595710 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:10732809 PMID:15064763 PMID:16714318 PMID:16835246 PMID:17215403 PMID:17296794 PMID:18602827 PMID:21149811 PMID:21772703 PMID:22492563 PMID:24863639 PMID:24957169 PMID:25741868 PMID:26467025 PMID:26989944 PMID:27025386 PMID:27027447 PMID:27088055 PMID:27265096 PMID:27549087 PMID:27863451 PMID:28286897 PMID:28492532 PMID:28660751 PMID:30340945 PMID:31211173 PMID:31372974 PMID:31832804


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595719 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:18458227 PMID:20008656 PMID:20350294 PMID:20482598 PMID:22492563 PMID:24033266 PMID:24126688 PMID:25025039 PMID:25741868 PMID:26085578 PMID:26114802 PMID:28251916 PMID:28414270 PMID:28492532 PMID:29358271 PMID:30158064 PMID:33415332 PMID:33502018


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:155801085 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:18458227 PMID:20008656 PMID:25741868 PMID:26114802 PMID:26467025 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:10408904 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16087932 PMID:16714318 PMID:16835246 PMID:17309650 PMID:20951041 PMID:24126688 PMID:24819634 PMID:25741868 PMID:26467025 PMID:27549087 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:151745152 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:24863639 PMID:25741868 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595716 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16437557 PMID:16714318 PMID:20008656 PMID:24819634 PMID:25741868 PMID:26147798 PMID:26467025 PMID:30442897 PMID:31372974 PMID:31832804


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:13827488 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:25741868 PMID:25741909 PMID:28492532 PMID:32657593 PMID:33415332 PMID:34193129


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:14699991 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16762064 PMID:25741868 PMID:28215760 PMID:28492532 PMID:33841295 PMID:34354735


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595717 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:15549395 PMID:16437557 PMID:16762064 PMID:16835246 PMID:17444508 PMID:18996695 PMID:20008656 PMID:20301684 PMID:20350294 PMID:20587496 PMID:21508331 PMID:21707411 PMID:22206013 PMID:22492563 PMID:22762946 PMID:24604904 PMID:24819634 PMID:25448007 PMID:25741868 PMID:25802885 PMID:26085578 PMID:26467025 PMID:27549087 PMID:28063088 PMID:28492532 PMID:29898954 PMID:31673878


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:151806788|RGD:8691947|RGD:8691957 (Homo sapiens) & RGD:151806788|RGD:8691947|RGD:8691957 (Homo sapiens) & RGD:151806788|RGD:8691947|RGD:8691957 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:10408933 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:16762064 PMID:16835246 PMID:19889647 PMID:22492563 PMID:22851605 PMID:22926664 PMID:24473995 PMID:24957169 PMID:25741868 PMID:26467025 PMID:26801520 PMID:28251916 PMID:28492532 PMID:29674596 PMID:30649465 PMID:31664033


    • An association has been curated linking MFN2 and Charcot-Marie-Tooth disease type 2A2A 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:8595707 (Homo sapiens)
  • 2 RGD objects have been annotated to Charcot-Marie-Tooth disease type 2A2A  (DOID:0110155)
  • 52 papers in RGD have been used to annotate MFN2
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, type 2A2A
  • Original References(s): PMID:15064763 PMID:15549395 PMID:16714318 PMID:17215403 PMID:17296794 PMID:17437620 PMID:18996695 PMID:19812251 PMID:19889647 PMID:20335458 PMID:20350294 PMID:20418531 PMID:21285398 PMID:21508331 PMID:22442078 PMID:22492563 PMID:24604904 PMID:25025039 PMID:25741868 PMID:26230519 PMID:26467025 PMID:28492532 PMID:29266326 PMID:29898954 PMID:30340945 PMID:30659145 PMID:30882371 PMID:31186069 PMID:31640251 PMID:31832804 PMID:34103343 PMID:35418194 PMID:9409358


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