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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Tpp1 and autosomal recessive spinocerebellar ataxia 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 TPP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 7  (DOID:0080059)
  • 14 papers in RGD have been used to annotate Tpp1


    • An association has been curated linking Tpp1 and autosomal recessive spinocerebellar ataxia 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 TPP1 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 7  (DOID:0080059)
  • 14 papers in RGD have been used to annotate Tpp1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Tpp1 and autosomal recessive spinocerebellar ataxia 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 TPP1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal recessive spinocerebellar ataxia 7  (DOID:0080059)
  • 14 papers in RGD have been used to annotate Tpp1
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive spinocerebellar ataxia 7 | ClinVar Annotator: match by term: Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia | ClinVar Annotator: match by term: TPP1-related condition
  • Original References(s): PMID:10330339 PMID:10862088 PMID:11017954 PMID:11071145 PMID:11339651 PMID:12376936 PMID:12414822 PMID:12488460 PMID:12796825 PMID:12950156 PMID:15317752 PMID:15520412 PMID:16199547 PMID:16782851 PMID:16814585 PMID:17576681 PMID:17679671 PMID:17959406 PMID:18283468 PMID:18473686 PMID:18684116 PMID:19038966 PMID:19038967 PMID:19201763 PMID:19246452 PMID:19793312 PMID:20301601 PMID:20340139 PMID:21990111 PMID:22245569 PMID:22612257 PMID:22752289 PMID:23266810 PMID:23418007 PMID:23539563 PMID:25326635 PMID:25356970 PMID:25525159 PMID:25741868 PMID:26026925 PMID:26075876 PMID:26224725 PMID:26467025 PMID:26795593 PMID:27407112 PMID:27553520 PMID:28335910 PMID:28464005 PMID:28492532 PMID:29631617 PMID:29655203 PMID:29687370 PMID:30119717 PMID:30771299 PMID:31122803 PMID:31283065 PMID:31489614 PMID:32329550 PMID:32412666 PMID:32855042 PMID:34126256 PMID:36403551 PMID:9295267 PMID:9536098 PMID:9788728


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