Symbol Name ID |
Gja1
gap junction protein, alpha 1 MGI:95713 |
Darker colors indicate more annotations |
Human Phenotypes | Uveitis |
Skin rash |
Disease(s) Associated with GJA1 | ||
erythrokeratodermia variabilis | ||
oculodentodigital dysplasia |
Mouse Phenotypes | heart inflammation |
abnormal neutrophil physiology |
abnormal lymphatic vessel morphology |
absent lymphatic vessels |
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Availability | Mouse Genotype | ||||
Gja1M1Jrt/Gja1+ | |||||
Gja1tm1.1Kwi/Gja1+ | |||||
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 05/21/2024 MGI 6.23 |
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