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Symbol Name ID |
Nkx2-5
NK2 homeobox 5 MGI:97350 |
| Darker colors indicate more annotations |
| Human Phenotypes | Umbilical hernia |
| Disease(s) Associated with NKX2-5 | |
| congenital nongoitrous hypothyroidism 5 |
| Mouse Phenotypes | right atrial isomerism |
enlarged heart |
cardiac hypertrophy |
embryonic growth retardation |
decreased embryo size |
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| Availability | Mouse Genotype | |||||
| Nkx2-5tm1.1Burg/Nkx2-5tm1.1Burg | ||||||
| Nkx2-5tm1.1Hkas/Nkx2-5tm1.1Hkas | ||||||
| Nkx2-5tm1Siz/Nkx2-5tm1Siz | ||||||
| Nkx2-5tm1Wehi/Nkx2-5tm1Wehi | ||||||
| Nkx2-5tm1.1Hkas/Nkx2-5+ | ||||||
| Myl2tm1(cre)Krc/Myl2+ Nkx2-5tm1Krc/Nkx2-5tm1Krc (conditional) |
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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 07/02/2024 MGI 6.13 |
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