Symbol Name ID |
Casr
calcium-sensing receptor MGI:1351351 |
Darker colors indicate more annotations |
Human Phenotypes | Fatigable weakness |
Basal ganglia calcification |
Myoclonus |
Cortical myoclonus |
Increased intracranial pressure |
Depression |
Emotional lability |
Anxiety |
Atypical behavior |
Reduced consciousness |
Writer's cramp |
Seizure |
Bilateral tonic-clonic seizure |
Focal impaired awareness seizure |
Generalized non-motor (absence) seizure |
Febrile seizure (within the age range of 3 months to 6 years) |
Paresthesia |
Disease(s) Associated with CASR | |||||||||||||||||
autosomal dominant hypocalcemia | |||||||||||||||||
autosomal dominant hypocalcemia 1 | |||||||||||||||||
idiopathic generalized epilepsy 8 |
Mouse Phenotypes | small superior vagus ganglion |
decreased prepulse inhibition |
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Availability | Mouse Genotype | ||
Casrtm1b(KOMP)Mbp/Casr+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 07/05/2024 MGI 6.24 |
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