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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G in Mus musculus.        

  • 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in RGD have been used to annotate Tcap


    • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G in Mus musculus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • 1 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in RGD have been used to annotate Tcap
  • Curation Notes: OMIM:601954


    • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G in Mus musculus.        

  • 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 TCAP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in RGD have been used to annotate Tcap
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy type 2G | ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 2G
  • Original References(s): PMID:10655062 PMID:15582318 PMID:16352453 PMID:16911908 PMID:17097056 PMID:18414213 PMID:18585512 PMID:18948002 PMID:19035361 PMID:19412328 PMID:20215591 PMID:20474083 PMID:21530252 PMID:22194935 PMID:23299917 PMID:23479141 PMID:23861362 PMID:24033266 PMID:24037902 PMID:24503780 PMID:25055047 PMID:25298746 PMID:25326637 PMID:25351510 PMID:25741868 PMID:26084686 PMID:26332198 PMID:26350513 PMID:26467025 PMID:27055092 PMID:27532257 PMID:27618135 PMID:28492532 PMID:28518168 PMID:28771489 PMID:29447731 PMID:29884292 PMID:29935994 PMID:30531895 PMID:30564623 PMID:30847666 PMID:30871747 PMID:31114860 PMID:31303467 PMID:31980526 PMID:31983221 PMID:32140910 PMID:32233023 PMID:32451364 PMID:32528171 PMID:32880476 PMID:34540776 PMID:35026164


    • An association has been curated linking Tcap and autosomal recessive limb-girdle muscular dystrophy type 2G in Mus musculus.        

  • 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 TCAP (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive limb-girdle muscular dystrophy type 2G  (DOID:0110281)
  • 4 papers in RGD have been used to annotate Tcap
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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