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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11601971 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:19:25.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11549499 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive
  • Original References(s): PMID:25741868

  • This annotation was curated on 2020-03-26 10:18:03.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11653683 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:19:28.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11661682 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:18:32.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:8691414 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:17:37.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11660178 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:19:23.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11605542 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:19:30.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:10411712 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:15:20.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:11601479 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive

  • This annotation was curated on 2020-03-26 10:19:07.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:8691412 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:37.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:10051649 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:15:24.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:10410570 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2020-03-26 10:14:45.0 by RGD . For more information contact us

    An association has been curated linking TMEM126A and Hereditary Optic Atrophies 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:8691413 (Homo sapiens)
  • 65 RGD objects have been annotated to Hereditary Optic Atrophies  (DOID:9005850)
  • 4 papers in RGD have been used to annotate TMEM126A
  • Curation Notes: ClinVar Annotator: match by term: Optic Atrophy, Recessive
  • Original References(s): PMID:28492532

  • This annotation was curated on 2020-03-26 10:17:37.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.