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Pathways

MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:tremors
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Accession:MP:0000745 term browser browse the term
Definition:repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement
Synonyms:exact_synonym: quivering;   shaking;   trembling;   tremor
 related_synonym: Shivering
 xref: HP:0025144



show annotations for term's descendants           Sort by:
tremors term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp2b3 ATPase plasma membrane Ca2+ transporting 3 IAGP RGD PMID:27013529 RGD:13825260 NCBI chr  X:156,367,582...156,464,085
Ensembl chr  X:156,367,852...156,438,153
JBrowse link
G Atrn attractin IAGP DNA:deletion:exon RGD PMID:12379762 PMID:11209055 RGD:1299186, RGD:67998 NCBI chr 3:138,563,271...138,697,360
Ensembl chr 3:138,563,312...138,697,360
JBrowse link
G Kcnn2 potassium calcium-activated channel subfamily N member 2 IMP DNA:missense mutation:cds:c. 866T>A (p. I289N)(rat) RGD PMID:28917524 RGD:38508907 NCBI chr18:40,004,693...40,445,043
Ensembl chr18:40,155,939...40,445,045
JBrowse link
G Kcnn2Trdk potassium calcium-activated channel subfamily N member 2; Trdk mutant IMP DNA:missense mutation:cds:c. 866T>A (p. I289N)(rat) RGD PMID:28917524 RGD:38508907
G Plp1 proteolipid protein 1 IAGP RGD PMID:434110 PMID:2479544 RGD:1358782, RGD:1358781 NCBI chr  X:104,933,921...104,993,317
Ensembl chr  X:104,975,780...104,993,314
JBrowse link
G Plp1md proteolipid protein 1; Myelin-deficient IAGP RGD PMID:2479544 RGD:1358781
G Tubb4a tubulin, beta 4A class IVa IAGP DNA:missense mutation:cds:p.Ala302Thr (rat) RGD PMID:28393430 RGD:150429639 NCBI chr 9:2,004,836...2,012,281
Ensembl chr 9:2,004,840...2,012,286
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  mammalian phenotype 5432
    behavior/neurological phenotype 622
      abnormal behavior 621
        abnormal motor capabilities/coordination/movement 240
          abnormal involuntary movement 75
            tremors 18
paths to the root