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GENE - TERM ANNOTATION REPORT

23 Annotations Found.

An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:126909932 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:25741868 PMID:31673878


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8564010 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:19158810


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8567930 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:20039262


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:28907408 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:24078732 PMID:28492532 PMID:28501821


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:11608547 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:19158810 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8622570 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, demyelinating, type 1f
  • Original References(s): PMID:16930284 PMID:17052987 PMID:20039262 PMID:25741868 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8622561 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: CMT 1F
  • Original References(s): PMID:12477167 PMID:25741868 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:10766857 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28501821


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8571056 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:12477167 PMID:19123978 PMID:20301384 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:13477821 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, demyelinating, type 1f
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8571055 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:12477167 PMID:12566280 PMID:19158810 PMID:20301384 PMID:21840889 PMID:25448007 PMID:25552649 PMID:25741868 PMID:25741869 PMID:26645395 PMID:27206872 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8564005 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, demyelinating, type 1f
  • Original References(s): PMID:12481988 PMID:15111691 PMID:16452125 PMID:18023247 PMID:19286384 PMID:20421365 PMID:21168446 PMID:21493625 PMID:2288874 PMID:23230147 PMID:25741868 PMID:26467025 PMID:28492532 PMID:28501821 PMID:31211173 PMID:31574566


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8622549|RGD:8622552 (Homo sapiens) & RGD:8622549|RGD:8622552 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:12566280 PMID:25741868 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:10405615|RGD:11094207|RGD:151890891 (Homo sapiens) & RGD:10405615|RGD:11094207|RGD:151890891 (Homo sapiens) & RGD:10405615|RGD:11094207|RGD:151890891 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:8571057|RGD:8571058 (Homo sapiens) & RGD:8571057|RGD:8571058 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:20301384


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:151348564|RGD:596923512 (Homo sapiens) & RGD:151348564|RGD:596923512 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:25741868 PMID:29888333


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:11655052|RGD:28872542|RGD:28909796|RGD:8622568 (Homo sapiens) & RGD:11655052|RGD:28872542|RGD:28909796|RGD:8622568 (Homo sapiens) & RGD:11655052|RGD:28872542|RGD:28909796|RGD:8622568 (Homo sapiens) & RGD:11655052|RGD:28872542|RGD:28909796|RGD:8622568 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:13446166 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:19158810 PMID:20039262 PMID:25741868 PMID:28492532


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens) & RGD:14716380|RGD:28868447|RGD:28872732|RGD:28909804|RGD:38457368|RGD:38459762|RGD:401855725 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:25741868


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens) & RGD:11601942|RGD:11602406|RGD:11603218|RGD:11604205|RGD:11606073|RGD:11609130|RGD:11611109|RGD:11611808|RGD:11654975|RGD:11657547|RGD:11658304|RGD:11658736|RGD:11660356|RGD:11661537|RGD:11663842|RGD:11664070|RGD:28868113|RGD:28868450|RGD:28868452|RGD:28872286|RGD:28872288|RGD:28907409|RGD:28909514|RGD:28909516|RGD:28909643|RGD:28909799|RGD:28909801|RGD:28909802 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F


    • An association has been curated linking NEFL and Charcot-Marie-Tooth disease type 1F 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:10767629 (Homo sapiens)
  • 1 RGD objects have been annotated to Charcot-Marie-Tooth disease type 1F  (DOID:0110149)
  • 45 papers in RGD have been used to annotate NEFL
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease type 1F
  • Original References(s): PMID:12481988 PMID:15111691 PMID:16452125 PMID:19286384 PMID:21168446 PMID:25741868 PMID:26467025 PMID:28492532 PMID:31947737


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