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GENE - TERM ANNOTATION REPORT

66 Annotations Found.

An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542167 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25568300 PMID:26235739


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542182 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:26297079


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10051042 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26993267 PMID:28492532 PMID:29100083 PMID:33201365


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:9686541 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25239001


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:13210929 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:28708303


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542171 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25533962


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542172 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25914188 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542176 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25818041


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542164 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25568300


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8660630 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:18414213 PMID:26220391 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542179 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:26235739


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542166 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:26235738


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542183 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:23934111


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8660631 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:18414213 PMID:25568300


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542169 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25568300 PMID:26297079 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542186 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:23934111 PMID:25741868


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:15040447 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:31680123


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:13530931 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:22365152 PMID:26680202


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:21404380 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:26993267


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8692808 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542178 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:24874546 PMID:25849321 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542170 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25533962 PMID:25568300 PMID:28135719 PMID:28492532 PMID:32916281


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8660634 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:18414213 PMID:25741868 PMID:27210545 PMID:27875746 PMID:28492532 PMID:34431999


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8602133 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:22365152 PMID:25227913 PMID:27267376 PMID:28492532 PMID:28676574 PMID:29186148


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8688697 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:12374766 PMID:17881658 PMID:22365152 PMID:25326635 PMID:25326637 PMID:25741868 PMID:25785782 PMID:26235739 PMID:27779742 PMID:28492532 PMID:28923014 PMID:29186148 PMID:29720203 PMID:30171078 PMID:31715021


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542173 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:24888894 PMID:25568300 PMID:25741868 PMID:25951352 PMID:26029160 PMID:26647175 PMID:26900580 PMID:27779742 PMID:28387369 PMID:28492532 PMID:31715021


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10398263 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:24888894 PMID:25568300 PMID:25741868 PMID:25951352 PMID:26029160 PMID:26900580 PMID:28492532 PMID:31402610


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542165 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:24888894 PMID:25741868 PMID:34431999


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8621337 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:23708187 PMID:27267376


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10398251 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:27864847 PMID:28492532 PMID:28923014 PMID:30171078 PMID:30615093 PMID:31402610


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:9589516 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:15525788 PMID:15800189 PMID:19465131 PMID:20869590 PMID:23020937 PMID:24888894 PMID:25046240 PMID:25568300 PMID:25785782 PMID:26029160 PMID:26235739 PMID:26900580 PMID:28492532 PMID:28735751 PMID:29588952 PMID:31715021


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10401331 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:24194747 PMID:24874546 PMID:25741868 PMID:28492532 PMID:30171078 PMID:31715021


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:405136149 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:28492532 PMID:35188110


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10448448 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:23708187 PMID:25741868


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10046785 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25725044 PMID:25741868 PMID:26029160 PMID:26467025 PMID:26900580 PMID:27165006 PMID:28492532 PMID:29100083 PMID:31026061


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:13517367 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:31780880


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:151821728 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26993267 PMID:28492532 PMID:29100083


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10046784 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25725044 PMID:25741868 PMID:32581362


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10398245 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29655203


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:153346134 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:31904124 PMID:32845893 PMID:35599849


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:150337548 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25666757 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:12893963 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29263050 PMID:29655203 PMID:31904124


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:126758704 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542184 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25785782 PMID:26235739 PMID:26252990 PMID:26297079 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:38598118 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:23020937 PMID:25046240 PMID:25568300 PMID:25741868 PMID:25785782 PMID:28492532 PMID:29588952 PMID:29720203


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:26902677 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25568300 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:150556980 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:27875746 PMID:28492532 PMID:32901917


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11531406 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26677014 PMID:28492532 PMID:30185235 PMID:30615093


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens) & RGD:11051324|RGD:126909506|RGD:127287814|RGD:12738944|RGD:12741882|RGD:13469674|RGD:151233781|RGD:151661281|RGD:151663348|RGD:21070362|RGD:21070365|RGD:21070374|RGD:38464776|RGD:405280971|RGD:405281543|RGD:40903455 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens) & RGD:10396845|RGD:10398250|RGD:10398267|RGD:11552531|RGD:11613573|RGD:11638233|RGD:126744563|RGD:126766710|RGD:127316559|RGD:12849176|RGD:12894200|RGD:13216211|RGD:13462461|RGD:13494278|RGD:13528029|RGD:13612129|RGD:13620487|RGD:13704293|RGD:13811854|RGD:14399200|RGD:14696543|RGD:14719348|RGD:14741716|RGD:151725797|RGD:151754250|RGD:151776151|RGD:151778997|RGD:155800272|RGD:155913204|RGD:156191914|RGD:243051048|RGD:26912833|RGD:38460977|RGD:38463002|RGD:38482345|RGD:38598466|RGD:401830811|RGD:8660624|RGD:8692811 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13 | ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542177 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:24352161 PMID:25741868 PMID:25799905 PMID:26467025 PMID:26993267 PMID:27375106 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:151851125 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:28492532 PMID:30951195


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:127259000 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26993267 PMID:28492532 PMID:29432985 PMID:31026061


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:13508838 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:28492532 PMID:28973083 PMID:30078772 PMID:31026061


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11642593 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:28492532 PMID:35701389


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542181|RGD:150557002 (Homo sapiens) & RGD:11542181|RGD:150557002 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:24888894 PMID:25568300 PMID:25741868


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8660626|RGD:8692805 (Homo sapiens) & RGD:8660626|RGD:8692805 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26467025 PMID:27875746 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:10398252|RGD:11542175 (Homo sapiens) & RGD:10398252|RGD:11542175 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25568300 PMID:25741868


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:153345828|RGD:155798894 (Homo sapiens) & RGD:153345828|RGD:155798894 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:25741868 PMID:31904124


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542180|RGD:9589517|RGD:9589518 (Homo sapiens) & RGD:11542180|RGD:9589517|RGD:9589518 (Homo sapiens) & RGD:11542180|RGD:9589517|RGD:9589518 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13
  • Original References(s): PMID:24888894


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:11542168|RGD:11542174 (Homo sapiens) & RGD:11542168|RGD:11542174 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25568300 PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:13620262|RGD:13803183|RGD:14705522 (Homo sapiens) & RGD:13620262|RGD:13803183|RGD:14705522 (Homo sapiens) & RGD:13620262|RGD:13803183|RGD:14705522 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:28492532


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens) & RGD:126731471|RGD:126731475|RGD:126731484|RGD:126744676|RGD:12743050|RGD:12791953|RGD:13215412|RGD:13786201|RGD:14716778|RGD:15040514|RGD:150438175|RGD:150452660|RGD:150452779|RGD:150493611|RGD:150513978|RGD:150520444|RGD:150529833|RGD:150534720|RGD:150553817|RGD:152999514|RGD:155268359|RGD:155710484|RGD:155800262|RGD:155800267|RGD:155800270|RGD:155801052|RGD:156200485|RGD:21070371|RGD:21404274|RGD:21404426|RGD:243055970|RGD:25319108|RGD:26903072|RGD:26903075|RGD:26903077|RGD:26903082|RGD:28876064|RGD:38459540|RGD:38462541|RGD:38596910|RGD:38597705|RGD:38598463|RGD:38598522|RGD:401828211|RGD:401856278|RGD:401875184|RGD:401965322|RGD:40815358|RGD:40815359|RGD:42724007 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Developmental and epileptic encephalopathy, 13 | ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868


    • An association has been curated linking SCN8A and developmental and epileptic encephalopathy 13 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:8660628|RGD:8660629|RGD:8660633|RGD:8660635 (Homo sapiens) & RGD:8660628|RGD:8660629|RGD:8660633|RGD:8660635 (Homo sapiens) & RGD:8660628|RGD:8660629|RGD:8660633|RGD:8660635 (Homo sapiens) & RGD:8660628|RGD:8660629|RGD:8660633|RGD:8660635 (Homo sapiens)
  • 18 RGD objects have been annotated to developmental and epileptic encephalopathy 13  (DOID:0080445)
  • 6 papers in RGD have been used to annotate SCN8A
  • Curation Notes: ClinVar Annotator: match by term: Early infantile epileptic encephalopathy 13
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


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