Symbol Name ID |
Gja1
gap junction protein, alpha 1 MGI:95713 |
Darker colors indicate more annotations |
Human Phenotypes | Maternal diabetes |
Abnormality of chromosome segregation |
Hypoglycemia |
Diabetes mellitus |
Cerebral calcification |
Basal ganglia calcification |
Disease(s) Associated with GJA1 | ||||||
erythrokeratodermia variabilis | ||||||
hypoplastic left heart syndrome | ||||||
oculodentodigital dysplasia |
Mouse Phenotypes | abnormal vascular wound healing |
abnormal blood homeostasis |
abnormal circulating hormone level |
cyanosis |
edema |
lymphedema |
impaired skin barrier function |
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Availability | Mouse Genotype | |||||||
Gja1tm1Kdr/Gja1tm1Kdr | ||||||||
Gja1tm3.1Clo/Gja1tm3.1Clo | ||||||||
Gja1tm4Kwi/Gja1tm4Kwi | ||||||||
Gja1tm1Dlg/Gja1tm1Dlg Tg(Tek-cre)1Ywa/0 (conditional) |
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Gja1tm1Kwi/Gja1+ Tg(KRT5-cre)5132Jlj/0 (conditional) |
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Gja1tm1Kwi/Gja1tm5(cre/ERT)Kwi (conditional) |
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 04/09/2024 MGI 6.23 |
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