Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References FTP Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper Genome Scanner
Aging & Age-Related Disease Cancer Cardiovascular Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Genetic Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking SLC17A8 and autosomal dominant nonsyndromic deafness 25 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:12907383 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 12 papers in RGD have been used to annotate SLC17A8
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 25
  • Original References(s): PMID:23967202, PMID:25741868

    • This annotation was curated on 2019-11-12 07:30:55.0 by RGD . For more information contact us

    An association has been curated linking SLC17A8 and autosomal dominant nonsyndromic deafness 25 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 autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 12 papers in RGD have been used to annotate SLC17A8

    • This annotation was curated on 2019-11-27 19:57:11.0 by RGD . For more information contact us

    An association has been curated linking SLC17A8 and autosomal dominant nonsyndromic deafness 25 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:8596030 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 12 papers in RGD have been used to annotate SLC17A8
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 25
  • Original References(s): PMID:18674745

    • This annotation was curated on 2019-11-12 07:31:26.0 by RGD . For more information contact us

    An association has been curated linking SLC17A8 and autosomal dominant nonsyndromic deafness 25 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:14693486 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 25  (DOID:0110555)
  • 12 papers in RGD have been used to annotate SLC17A8
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 25

    • This annotation was curated on 2019-11-12 07:28:13.0 by RGD . For more information contact us

    Go Back to source page   Continue to Ontology report



    Contact Us |  About Us |  License CC BY 4.0 |  Legal Disclaimer |  © Medical College of Wisconsin
    NHLBI Logo

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