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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 spleen morphology |
abnormal neutrophil physiology |
abnormal osteoclast physiology |
abnormal lymphatic vessel morphology |
absent lymphatic vessels |
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| Availability | Mouse Genotype | ||||||
| Gja1em1Ipche/Gja1em1Ipche | |||||||
| Gja1em1(IMPC)Ccpcz/Gja1+ | |||||||
| 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 06/09/2026 MGI 6.24 |
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