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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking LOC129931512 and dyschromatosis symmetrica hereditaria 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:10049382 (Homo sapiens)
  • 9 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate LOC129931512
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC129931512 and dyschromatosis symmetrica hereditaria 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:38466203 (Homo sapiens)
  • 9 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate LOC129931512
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29221912


    • An association has been curated linking LOC129931512 and dyschromatosis symmetrica hereditaria 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:11598441 (Homo sapiens)
  • 9 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate LOC129931512
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities


    • An association has been curated linking LOC129931512 and dyschromatosis symmetrica hereditaria 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:126731478|RGD:151710112|RGD:156236771 (Homo sapiens) & RGD:126731478|RGD:151710112|RGD:156236771 (Homo sapiens) & RGD:126731478|RGD:151710112|RGD:156236771 (Homo sapiens)
  • 9 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate LOC129931512
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking LOC129931512 and dyschromatosis symmetrica hereditaria 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:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens) & RGD:126759401|RGD:151830868|RGD:152042040|RGD:152057807|RGD:152076416|RGD:152142414|RGD:152174593|RGD:156081578|RGD:156115729|RGD:402517602|RGD:402520606|RGD:402521882|RGD:405007986|RGD:405069196 (Homo sapiens)
  • 9 RGD objects have been annotated to dyschromatosis symmetrica hereditaria  (DOID:0060257)
  • 0 papers in RGD have been used to annotate LOC129931512
  • Curation Notes: ClinVar Annotator: match by term: Symmetrical dyschromatosis of extremities
  • Original References(s): PMID:28492532


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