Symbol Name ID |
Gnaq
guanine nucleotide binding protein, alpha q polypeptide MGI:95776 |
Darker colors indicate more annotations |
Human Phenotypes | Edema |
Cerebral calcification |
Disease(s) Associated with GNAQ | ||
familial multiple nevi flammei | ||
Sturge-Weber syndrome |
Mouse Phenotypes | abnormal platelet physiology |
decreased platelet aggregation |
abnormal blood coagulation |
abnormal atrial thrombosis |
increased bleeding time |
edema |
abnormal enzyme/coenzyme activity |
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Availability | Mouse Genotype | |||||||
Gnaqtm1Soff/Gnaqtm1Soff | ||||||||
Gnaqtm2.1Soff/Gnaqtm2.1Soff | ||||||||
Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne | ||||||||
Tg(Myh6-Gnaq*Q209L/Esr1*)7Rzl/0 | ||||||||
Tg(Myh6-Gnaq*Q209L)52Ejne/? |
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 04/16/2024 MGI 6.23 |
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