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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8596109 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:12145746 PMID:19438934 PMID:25741868 PMID:30303587 PMID:30311386 PMID:8593615


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8557394 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:12145746


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:9688176 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:24033266 PMID:24875298 PMID:28492532


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8596111 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:19438934


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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 autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8596108 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:12145746 PMID:30303587


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:153000390 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:30311386 PMID:35710363


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8596110 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:12145746 PMID:25741868


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:12742868 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:16389551 PMID:24416283 PMID:25741868 PMID:28492532


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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 autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:8610825|RGD:8610826|RGD:9692264 (Homo sapiens) & RGD:8610825|RGD:8610826|RGD:9692264 (Homo sapiens) & RGD:8610825|RGD:8610826|RGD:9692264 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:11088449|RGD:8610822 (Homo sapiens) & RGD:11088449|RGD:8610822 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6 | ClinVar Annotator: match by term: TMIE-related condition
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:28874935 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6
  • Original References(s): PMID:28492532


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens) & RGD:11581237|RGD:11584424|RGD:11585995|RGD:11586177|RGD:11588847|RGD:11590090|RGD:11591658|RGD:11592533|RGD:11594377|RGD:11595667|RGD:11595758|RGD:11645030|RGD:11653268|RGD:11661833|RGD:28870689|RGD:28870693|RGD:28870694|RGD:28870890|RGD:28874942|RGD:28877459|RGD:28877464|RGD:28877469|RGD:28877474|RGD:28877477|RGD:28882331|RGD:28882336|RGD:28882339|RGD:28882345 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6 | ClinVar Annotator: match by term: NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 6


    • An association has been curated linking TMIE and autosomal recessive nonsyndromic deafness 6 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:126909473|RGD:150336184|RGD:151661537|RGD:401722469 (Homo sapiens) & RGD:126909473|RGD:150336184|RGD:151661537|RGD:401722469 (Homo sapiens) & RGD:126909473|RGD:150336184|RGD:151661537|RGD:401722469 (Homo sapiens) & RGD:126909473|RGD:150336184|RGD:151661537|RGD:401722469 (Homo sapiens)
  • 1 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 6  (DOID:0110512)
  • 7 papers in RGD have been used to annotate TMIE
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 6 | ClinVar Annotator: match by term: TMIE-related condition
  • Original References(s): PMID:25741868


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