Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking SPG7 and frontotemporal dementia and/or amyotrophic lateral sclerosis 2 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:8605002 (Homo sapiens)
  • 3 RGD objects have been annotated to frontotemporal dementia and/or amyotrophic lateral sclerosis 2  (DOID:0060214)
  • 0 papers in RGD have been used to annotate SPG7
  • Curation Notes: ClinVar Annotator: match by term: FTDALS2
  • Original References(s): PMID:16534102 PMID:17661097 PMID:18200586 PMID:18799786 PMID:20186691 PMID:20301286 PMID:20981092 PMID:21623769 PMID:22571692 PMID:22964162 PMID:22995991 PMID:23065789 PMID:23269439 PMID:23733235 PMID:24727571 PMID:24731568 PMID:25133958 PMID:25497598 PMID:25525159 PMID:25681447 PMID:25741868 PMID:26467025 PMID:26506339 PMID:26626314 PMID:27165006 PMID:27557734 PMID:27957547 PMID:28362824 PMID:28444220 PMID:28492532 PMID:28832565 PMID:29026558 PMID:29057857 PMID:29246844 PMID:29482223 PMID:29867446 PMID:29913018 PMID:29915382 PMID:30098094 PMID:30369941 PMID:30537300 PMID:31068484 PMID:31316545 PMID:31433872 PMID:31692161 PMID:31854126 PMID:31980526 PMID:32040484 PMID:32153140 PMID:32161564 PMID:32447552 PMID:32548275 PMID:32581362 PMID:32816195 PMID:32893728 PMID:32973427 PMID:33059505 PMID:33084218 PMID:33144682 PMID:33157434 PMID:33300680 PMID:33598982 PMID:33726816 PMID:33841295 PMID:34405107 PMID:34426522 PMID:34445196 PMID:34662886 PMID:34758253 PMID:34782662 PMID:35499206 PMID:35586535 PMID:35869996 PMID:35872528 PMID:36530930 PMID:37213040 PMID:37712079 PMID:37766787 PMID:38549004 PMID:39825153


  • Go Back to source page   Continue to Ontology report