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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking LOC126862864 and episodic ataxia type 2 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:13518509 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:26467025 PMID:28492532 PMID:34436362


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:151861600 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:25741868 PMID:28007337 PMID:28492532 PMID:30283815 PMID:31468518


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:8597973 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:19586927


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:8597963 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:11723274 PMID:14718690


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:10051230 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:22249839 PMID:25741868 PMID:27959697 PMID:28007337 PMID:28492532 PMID:29056246 PMID:29100083 PMID:30283815 PMID:31468518 PMID:31487502


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:405000407 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:151848361 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:13808573 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:401940263 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:25741868


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:11636788 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:156051942|RGD:26895354 (Homo sapiens) & RGD:156051942|RGD:26895354 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:10371528 PMID:19486177 PMID:25735478 PMID:27250579 PMID:28492532


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:150453277 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:25741868 PMID:28007337 PMID:28492532 PMID:29056246 PMID:29100083 PMID:30283815 PMID:31468518


  • An association has been curated linking LOC126862864 and episodic ataxia type 2 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:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens) & RGD:11633181|RGD:127239741|RGD:127248075|RGD:127254611|RGD:127266469|RGD:127307625|RGD:14701383|RGD:14717071|RGD:15135119|RGD:151731387|RGD:151743363|RGD:151779873|RGD:151780436|RGD:151850602|RGD:152130829|RGD:152132342|RGD:152174023|RGD:155803831|RGD:155971176|RGD:156173427|RGD:156258382|RGD:156401917|RGD:156404391|RGD:38483241|RGD:405014654|RGD:405027201|RGD:405077289|RGD:405082617|RGD:405088015 (Homo sapiens)
  • 98 RGD objects have been annotated to episodic ataxia type 2  (DOID:0050990)
  • 0 papers in RGD have been used to annotate LOC126862864
  • Curation Notes: ClinVar Annotator: match by term: Episodic ataxia type 2
  • Original References(s): PMID:28492532


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