|
Symbol Name ID |
Gnaq
guanine nucleotide binding protein, alpha q polypeptide MGI:95776 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Intracranial hemorrhage |
Abnormal cerebral vascular morphology |
Stroke |
Dysphagia |
Cerebral calcification |
Abnormal cranial nerve morphology |
Hydrocephalus |
Cerebral cortical atrophy |
Chiari malformation |
Hemiparesis |
Hemiplegia |
Abnormality of speech or vocalization |
Atypical behavior |
Autistic behavior |
Attention deficit hyperactivity disorder |
Intellectual disability |
Hyperreflexia |
Seizure |
| Disease(s) Associated with GNAQ | ||||||||||||||||||
| familial multiple nevi flammei | ||||||||||||||||||
| Sturge-Weber syndrome |
| Mouse Phenotypes | nervous system phenotype |
abnormal innervation |
abnormal nervous system electrophysiology |
abnormal afterhyperpolarization |
abnormal glutamate-mediated receptor currents |
absent long-term depression |
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| Availability | Mouse Genotype | ||||||
| Gnaqtm1Soff/Gnaqtm1Soff | * | ||||||
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 05/28/2024 MGI 6.13 |
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