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GENE - TERM ANNOTATION REPORT

15 Annotations Found.

An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27353947 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:31964843 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:33946315 PMID:34178978 PMID:34689181 PMID:34721897 PMID:34906470 PMID:36284460 PMID:36764454 PMID:36909829 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(EXP) inferred from experiment]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:18836446


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Syndromic retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:28041643 PMID:28166811 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:32037395 PMID:32728228 PMID:33090715 PMID:33576794 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degeneration
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32037395 PMID:32218477 PMID:32728228 PMID:33090715 PMID:33576794 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degeneration
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:34178978 PMID:34906470 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant/Recessive | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:34178978 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degeneration
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:31964843 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:33946315 PMID:34178978 PMID:34721897 PMID:34906470 PMID:36764454 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32728228 PMID:33090715 PMID:33576794 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Syndromic retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:287049 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32552793 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:34178978 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Syndromic retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degeneration
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:34178978 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:34178978 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa | ClinVar Annotator: match by term: Tapetoretinal degeneration
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:34178978 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Dominant | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27353947 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:31964843 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:33946315 PMID:34178978 PMID:34721897 PMID:34906470 PMID:36284460 PMID:36764454 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27353947 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:31964843 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:33946315 PMID:34178978 PMID:34689181 PMID:34721897 PMID:34906470 PMID:35672425 PMID:36284460 PMID:36764454 PMID:36909829 PMID:9536098 PMID:9585594


  • An association has been curated linking Vmn2r17 and retinitis pigmentosa 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 EYS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 626 RGD objects have been annotated to retinitis pigmentosa  (DOID:10584)
  • 1 papers in RGD have been used to annotate Vmn2r17
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive retinitis pigmentosa | ClinVar Annotator: match by term: Retinitis Pigmentosa, Recessive | ClinVar Annotator: match by term: Retinitis pigmentosa
  • Original References(s): PMID:16199547 PMID:17156103 PMID:17576681 PMID:18836446 PMID:18976725 PMID:18976726 PMID:20237254 PMID:2033377 PMID:20333770 PMID:20333771 PMID:20375346 PMID:20537394 PMID:21069908 PMID:21179430 PMID:21217109 PMID:21519034 PMID:22164218 PMID:22277662 PMID:22302105 PMID:22334370 PMID:22363543 PMID:22581970 PMID:23105016 PMID:23421333 PMID:23591405 PMID:24033266 PMID:24265693 PMID:24474277 PMID:24618324 PMID:24652164 PMID:24670872 PMID:24938718 PMID:25096270 PMID:25097241 PMID:25133751 PMID:25268133 PMID:25324289 PMID:25356976 PMID:25366773 PMID:25412400 PMID:25491159 PMID:25692139 PMID:25741868 PMID:25753737 PMID:26103963 PMID:26155838 PMID:26161267 PMID:26261414 PMID:26355662 PMID:26593283 PMID:26667666 PMID:26787102 PMID:26806561 PMID:26872967 PMID:27208204 PMID:27353947 PMID:27375351 PMID:27658286 PMID:27735924 PMID:28041643 PMID:28224992 PMID:28418496 PMID:28419563 PMID:28492532 PMID:28704921 PMID:28763560 PMID:28838317 PMID:29068140 PMID:29074561 PMID:29159838 PMID:29550188 PMID:29625443 PMID:29641573 PMID:29785639 PMID:30153090 PMID:30337596 PMID:30487145 PMID:30513137 PMID:30543658 PMID:30718709 PMID:30804660 PMID:31054281 PMID:31074760 PMID:31087526 PMID:31106028 PMID:31213501 PMID:31456290 PMID:31725169 PMID:31814702 PMID:31872526 PMID:31960602 PMID:31964843 PMID:32000842 PMID:32037395 PMID:32218477 PMID:32483926 PMID:32531858 PMID:32581362 PMID:32675063 PMID:32728228 PMID:33090715 PMID:33247286 PMID:33576794 PMID:33691693 PMID:33749171 PMID:33833316 PMID:33946315 PMID:34178978 PMID:34689181 PMID:34721897 PMID:34906470 PMID:35672425 PMID:35836572 PMID:36284460 PMID:36460718 PMID:36464167 PMID:36764454 PMID:36819107 PMID:36909829 PMID:9536098 PMID:9585594


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