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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:juvenile myoclonic epilepsy
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Accession:DOID:4890 term browser browse the term
Definition:A adolescence-adult electroclinical syndrome that is characterized by brief, involuntary twitching of a muscle or a group of muscles (myoclonus) early in the morning with onset between 12 and 18 years. (DO)
Synonyms:exact_synonym: Adolescent Myoclonic Epilepsies;   Adolescent Myoclonic Epilepsy;   EJM;   Impulsive Petit Mal Epilepsy;   JME;   JME (Juvenile Myoclonic Epilepsy);   Janz Impulsive Petit Mal;   Janz Juvenile Myoclonic Epilepsy;   Janz Syndrome;   Juvenile Myoclonic Epilepsies;   Juvenile Myoclonic Epilepsy of Janz;   impulsive petit mal
 narrow_synonym: EJM1;   JANZ SYNDROME MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1;   juvenile myoclonic epilepsy 1
 primary_id: MESH:D020190
 alt_id: MIM:254770
 xref: GARD:6808;   MIM:PS254770;   MONDO:0009696;   NCI:C84796;   ORDO:307;   ORDO:862
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
juvenile myoclonic epilepsy term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G BRD2 bromodomain containing 2 ISO DNA:SNPs:promoter (human) RGD PMID:12830434 RGD:1358444 NCBI chr12:2,534,034...2,546,029
Ensembl chr12:2,534,034...2,546,029 		JBrowse link
G CACNA1G calcium voltage-gated channel subunit alpha1 G ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar NCBI chr 9:26,481,148...26,544,511
Ensembl chr 9:26,481,652...26,544,845 		JBrowse link
G CACNB4 calcium voltage-gated channel auxiliary subunit beta 4 ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar PMID:10762541 PMID:25741868 PMID:26467025 PMID:27843123 PMID:28492532 NCBI chr19:52,987,170...53,116,410
Ensembl chr19:52,993,618...53,116,140
Ensembl chr19:52,993,618...53,116,140 		JBrowse link
G CAPRIN1 cell cycle associated protein 1 ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar PMID:25741868 PMID:35979925 NCBI chr18:33,695,371...33,733,688
Ensembl chr18:33,695,371...33,733,688 		JBrowse link
G CHRNA1 cholinergic receptor nicotinic alpha 1 subunit ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar PMID:25741868 PMID:28492532 NCBI chr36:18,726,243...18,742,505
Ensembl chr36:18,726,243...18,742,505 		JBrowse link
G EFHC1 EF-hand domain containing 1 susceptibility ISO ClinVar Annotator: match by term: EJM1 | ClinVar Annotator: match by term: Janz syndrome | ClinVar Annotator: match by term: Juvenile myoclonic epilepsy | ClinVar Annotator: match by term: Myoclonic Epilepsy, Juvenile, 1 OMIM
ClinVar		 PMID:8737649 PMID:12439895 PMID:15258581 PMID:16199547 PMID:16839746 More... NCBI chr12:20,068,287...20,131,621
Ensembl chr12:20,067,881...20,131,619 		JBrowse link
G GABRA1 gamma-aminobutyric acid type A receptor subunit alpha1 ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar PMID:26467025 NCBI chr 4:49,006,981...49,065,205
Ensembl chr 4:49,009,495...49,062,581 		JBrowse link
G HSD17B3 hydroxysteroid 17-beta dehydrogenase 3 ISO ClinVar Annotator: match by term: Juvenile myoclonic epilepsy ClinVar PMID:25741868 PMID:27899157 PMID:28492532 PMID:33468338 PMID:35432193 More... NCBI chr 1:70,551,013...70,586,364
Ensembl chr 1:70,487,334...70,586,368 		JBrowse link
G JRK Jrk helix-turn-helix protein ISO CTD Direct Evidence: marker/mechanism CTD PMID:11463517 NCBI chr13:36,754,771...36,767,799 JBrowse link
Idiopathic Generalized Epilepsy 11 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CLCN2 chloride voltage-gated channel 2 susceptibility ISO ClinVar Annotator: match by term: EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 2 | ClinVar Annotator: match by term: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8 | ClinVar Annotator: match by term: Epilepsy, idiopathic generalized, susceptibility to, 11 ClinVar
OMIM		 PMID:1521363 PMID:9536098 PMID:12612585 PMID:15252188 PMID:15505175 More... NCBI chr34:17,224,136...17,238,755
Ensembl chr34:17,223,215...17,239,621 		JBrowse link
Idiopathic Generalized Epilepsy 13 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G GABRA1 gamma-aminobutyric acid type A receptor subunit alpha1 ISO ClinVar Annotator: match by term: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 13 | ClinVar Annotator: match by term: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 5 | ClinVar Annotator: match by term: Epilepsy, idiopathic generalized, susceptibility to, 13 ClinVar
OMIM		 PMID:11992121 PMID:16530959 PMID:16569738 PMID:18414213 PMID:18534981 More... NCBI chr 4:49,006,981...49,065,205
Ensembl chr 4:49,009,495...49,062,581 		JBrowse link
Idiopathic Generalized Epilepsy 7 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CHRNA7 cholinergic receptor nicotinic alpha 7 subunit ISO ClinVar Annotator: match by term: Epilepsy, idiopathic generalized, susceptibility to, 7 ClinVar PMID:25326635 PMID:25741868 NCBI chr 3:36,852,082...37,164,930
Ensembl chr 3:36,852,543...36,978,399 		JBrowse link
G EFHC1 EF-hand domain containing 1 ISO ClinVar Annotator: match by term: Epilepsy, idiopathic generalized, susceptibility to, 7 ClinVar PMID:25741868 PMID:28492532 NCBI chr12:20,068,287...20,131,621
Ensembl chr12:20,067,881...20,131,619 		JBrowse link
G SCN3A sodium voltage-gated channel alpha subunit 3 ISO ClinVar Annotator: match by term: Epilepsy, idiopathic generalized, susceptibility to, 7 ClinVar PMID:25741868 NCBI chr36:10,300,091...10,405,361
Ensembl chr36:10,302,191...10,377,923 		JBrowse link
juvenile myoclonic epilepsy 10 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G CILK1 ciliogenesis associated kinase 1 susceptibility ISO ClinVar Annotator: match by term: CILK1-related condition ClinVar
OMIM		 PMID:25741868 PMID:28492532 NCBI chr12:20,453,322...20,511,463
Ensembl chr12:20,450,834...20,511,673 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15757
    syndrome 10623
      electroclinical syndrome 1507
        absence epilepsy 239
          adolescence-adult electroclinical syndrome 134
            juvenile myoclonic epilepsy 13
              Idiopathic Generalized Epilepsy 11 1
              Idiopathic Generalized Epilepsy 13 1
              Idiopathic Generalized Epilepsy 7 3
              juvenile myoclonic epilepsy 10 1
              juvenile myoclonic epilepsy 3 0
              juvenile myoclonic epilepsy 4 0
              juvenile myoclonic epilepsy 9 0
Path 2
Term Annotations click to browse term
  disease 15757
    disease of anatomical entity 15377
      nervous system disease 13506
        central nervous system disease 12077
          brain disease 11341
            epilepsy 2903
              electroclinical syndrome 1507
                absence epilepsy 239
                  adolescence-adult electroclinical syndrome 134
                    juvenile myoclonic epilepsy 13
                      Idiopathic Generalized Epilepsy 11 1
                      Idiopathic Generalized Epilepsy 13 1
                      Idiopathic Generalized Epilepsy 7 3
                      juvenile myoclonic epilepsy 10 1
                      juvenile myoclonic epilepsy 3 0
                      juvenile myoclonic epilepsy 4 0
                      juvenile myoclonic epilepsy 9 0
paths to the root