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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Tmc1 and autosomal recessive nonsyndromic deafness 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with TMC1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 7  (DOID:0110520)
  • 8 papers in RGD have been used to annotate Tmc1


    • An association has been curated linking Tmc1 and autosomal recessive nonsyndromic deafness 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with TMC1 (Homo sapiens) [(EXP) inferred from experiment]
  • 3 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 7  (DOID:0110520)
  • 8 papers in RGD have been used to annotate Tmc1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Tmc1 and autosomal recessive nonsyndromic deafness 7 in Rattus norvegicus.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Tmc1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 7  (DOID:0110520)
  • 8 papers in RGD have been used to annotate Tmc1
  • Curation Notes: OMIM:600974


    • An association has been curated linking Tmc1 and autosomal recessive nonsyndromic deafness 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • 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 from sequence orthology with TMC1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 7  (DOID:0110520)
  • 8 papers in RGD have been used to annotate Tmc1
  • Curation Notes: ClinVar Annotator: match by term: DEAFNESS, AUTOSOMAL RECESSIVE 11 | ClinVar Annotator: match by term: Deafness, autosomal recessive 7
  • Original References(s): PMID:11850618 PMID:16134132 PMID:16199547 PMID:16287143 PMID:17576681 PMID:17877751 PMID:18414213 PMID:18616530 PMID:19187973 PMID:20373850 PMID:21117948 PMID:21250555 PMID:21252500 PMID:21917145 PMID:22105175 PMID:22607986 PMID:23208854 PMID:23767834 PMID:24033266 PMID:24416283 PMID:24875298 PMID:24949729 PMID:25491636 PMID:25741868 PMID:25741915 PMID:26467025 PMID:26969326 PMID:27068579 PMID:28492532 PMID:29654653 PMID:30303587 PMID:31028865 PMID:31541171 PMID:31814694 PMID:31854501 PMID:32747562 PMID:33724713 PMID:34416374 PMID:34523024 PMID:9536098


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