Send us a Message



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

GENE - TERM ANNOTATION REPORT

24 Annotations Found.

An association has been curated linking PROM1 and retinitis pigmentosa 41 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:21071293 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:16199547 PMID:17605048 PMID:19718270 PMID:24154662 PMID:24516651 PMID:25474345 PMID:25741868 PMID:28492532 PMID:30588538 PMID:31129250 PMID:36909829


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:21071297 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:16199547 PMID:17605048 PMID:19718270 PMID:24154662 PMID:25474345 PMID:25741868 PMID:28492532 PMID:30578500 PMID:36909829


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:21071296 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:20042663 PMID:24154662 PMID:25474345 PMID:25741868 PMID:28492532 PMID:31129250 PMID:36909829


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:8558811 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:10587575


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:8596854 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:26872967 PMID:28041643


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:15017079 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:24154662 PMID:24938718 PMID:25474345 PMID:25741868 PMID:28492532 PMID:31054281


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:10045206 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868 PMID:26355662 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:12905773 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868 PMID:28418496 PMID:28492532 PMID:32531858


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:14396380 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:16199547 PMID:17605048 PMID:19718270 PMID:24154662 PMID:25474345 PMID:25741868 PMID:28492532 PMID:31199449


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:14695806 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:24154662 PMID:25474345 PMID:25741868 PMID:28492532 PMID:29343940 PMID:31054281


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:13435130 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:24154662 PMID:25356976 PMID:25474345 PMID:28041643 PMID:28492532 PMID:29555955


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:12742397 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:10205271 PMID:17605048 PMID:19718270 PMID:24154662 PMID:25474345 PMID:25741868 PMID:25999674 PMID:26103963 PMID:26261540 PMID:27874104 PMID:28041643 PMID:28492532 PMID:30588538


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:12858958 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:24154662 PMID:25472526 PMID:25474345 PMID:25741868 PMID:28492532 PMID:31129250


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:26909737 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868 PMID:28095140 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 in Homo sapiens.        

  • 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 Prom1 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: OMIM:612095


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:38493081 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17576681 PMID:28492532 PMID:30588538 PMID:9536098


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:10049983 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868 PMID:25910913 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:38493084 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:16199547 PMID:17605048 PMID:19718270 PMID:24154662 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:13795169|RGD:21071294 (Homo sapiens) & RGD:13795169|RGD:21071294 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:150453711|RGD:21071299|RGD:38477102 (Homo sapiens) & RGD:150453711|RGD:21071299|RGD:38477102 (Homo sapiens) & RGD:150453711|RGD:21071299|RGD:38477102 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:17605048 PMID:19718270 PMID:24154662 PMID:25474345 PMID:25741868 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:11551730|RGD:8642245|RGD:8642249 (Homo sapiens) & RGD:11551730|RGD:8642245|RGD:8642249 (Homo sapiens) & RGD:11551730|RGD:8642245|RGD:8642249 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PROM1 and retinitis pigmentosa 41 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:150457998|RGD:150486327|RGD:151348701|RGD:151348791 (Homo sapiens) & RGD:150457998|RGD:150486327|RGD:151348701|RGD:151348791 (Homo sapiens) & RGD:150457998|RGD:150486327|RGD:151348701|RGD:151348791 (Homo sapiens) & RGD:150457998|RGD:150486327|RGD:151348701|RGD:151348791 (Homo sapiens)
  • 1 RGD objects have been annotated to retinitis pigmentosa 41  (DOID:0110376)
  • 6 papers in RGD have been used to annotate PROM1
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa 41
  • Original References(s): PMID:25741868


  • Go Back to source page   Continue to Ontology report