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GENE - TERM ANNOTATION REPORT

24 Annotations Found.

An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:11254442


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8654637 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:11935341 PMID:12189496 PMID:14572144 PMID:15037685 PMID:16470554 PMID:21555057 PMID:22006981 PMID:24824219 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:13789164 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:15992519 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8596542 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:11935341 PMID:16470554 PMID:21555057 PMID:24824219 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:13704778 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:25741868


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8624575 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:11935341 PMID:15367490 PMID:18757878 PMID:21145992 PMID:25741868 PMID:27322623 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:12739656 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:16470554 PMID:19168821 PMID:24824219 PMID:25497041 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8596538 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:12850517 PMID:14615938 PMID:16470554 PMID:16504440 PMID:17077634 PMID:18757878 PMID:22006981 PMID:22382567 PMID:22975760 PMID:25741868 PMID:25796299 PMID:26392452 PMID:27081509 PMID:27322623 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:14711485 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:16199547 PMID:16470554 PMID:16652334 PMID:24824219 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:13785242 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:21160490 PMID:22416245 PMID:27322623 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8596543 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:12189496 PMID:18757878 PMID:22975760 PMID:23793458 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:13704779 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:12939431 PMID:16199547 PMID:16470554 PMID:24824219 PMID:25741868 PMID:27264811 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:26919932 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:16470554 PMID:24824219 PMID:25497041 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:12899309 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:21160490 PMID:22416245 PMID:25634434 PMID:25741868 PMID:27322623 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8602497 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:16652334 PMID:21145992 PMID:21160490 PMID:21624973 PMID:22416245 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:127328272 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11935341 PMID:12939431 PMID:16470554 PMID:18757878 PMID:22737209 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8596541 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:11935341 PMID:12189496 PMID:16470554 PMID:18757878 PMID:21145992 PMID:22405205 PMID:23793458 PMID:25333069 PMID:25741868 PMID:28492532 PMID:29758562


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens) & RGD:11545831|RGD:11627880|RGD:11629645|RGD:11630234|RGD:11636845|RGD:15101449|RGD:15127335|RGD:15141227|RGD:15152128|RGD:15162593|RGD:8601214|RGD:8601216|RGD:8660053|RGD:8660054|RGD:8660055|RGD:8660056|RGD:8660057|RGD:8660058 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Leukoencephalopathy with swelling and cysts | ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens) & RGD:11612984|RGD:11616342|RGD:11631270|RGD:127236050|RGD:127246115|RGD:15112602|RGD:15116605|RGD:15116627|RGD:15124347|RGD:15139477|RGD:15147143|RGD:15167722|RGD:15178745|RGD:15191168 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:8601217 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:12497630 PMID:16652334 PMID:25741868 PMID:28492532


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:127255660 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:11254442 PMID:11935341 PMID:16199547 PMID:16470554 PMID:24824219 PMID:25741868 PMID:28492532 PMID:32056211 PMID:33084218


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:151887000 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:12939431 PMID:18757878 PMID:24315536 PMID:25741868 PMID:27322623 PMID:28492532 PMID:34504271


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens) & RGD:11632264|RGD:11635335|RGD:11635585|RGD:11635645|RGD:11659370|RGD:150433130|RGD:150441890|RGD:150501623|RGD:40905616|RGD:40905617|RGD:40905618|RGD:40905619|RGD:40905620 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts


    • An association has been curated linking MLC1 and megalencephalic leukoencephalopathy with subcortical cysts 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:151352019|RGD:8624572 (Homo sapiens) & RGD:151352019|RGD:8624572 (Homo sapiens)
  • 6 RGD objects have been annotated to megalencephalic leukoencephalopathy with subcortical cysts  (DOID:0080315)
  • 5 papers in RGD have been used to annotate MLC1
  • Curation Notes: ClinVar Annotator: match by term: Megalencephalic leukoencephalopathy with subcortical cysts
  • Original References(s): PMID:15832614 PMID:16652334 PMID:25497041 PMID:25741868 PMID:28492532 PMID:31302377


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