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Symbol Name ID |
Hccs
holocytochrome c synthetase MGI:106911 |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital diaphragmatic hernia |
| Disease(s) Associated with HCCS | |
| linear skin defects with multiple congenital anomalies 1 |
| Mouse Phenotypes | decreased cardiac muscle glycogen level |
abnormal myocardium layer morphology |
dilated cardiomyopathy |
abnormal fetal cardiomyocyte proliferation |
decreased fetal cardiomyocyte proliferation |
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| Availability | Mouse Genotype | |||||
| Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ (conditional) |
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| Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ Tg(CAG-EGFP)D4Nagy/0 Tg(Hmgcr-lacZ)H253Sest/0 (conditional) |
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| Hccstm1Tcc/Y Nkx2-5tm2(cre)Rph/Nkx2-5+ (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 05/28/2024 MGI 6.13 |
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