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Symbol Name ID |
Hccs
holocytochrome c synthetase MGI:106911 |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital diaphragmatic hernia |
Short stature |
| Disease(s) Associated with HCCS | ||
| linear skin defects with multiple congenital anomalies 1 |
| Mouse Phenotypes | enlarged heart |
embryonic growth retardation |
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| Availability | Mouse Genotype | ||
| Arhgap6/Hccs/Mid1tm1Hzo/Arhgap6/Hccs/Mid1tm1Hzo Tg(EIIa-cre)C5379Lmgd/? (conditional) |
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| Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ (conditional) |
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| Arhgap6/Hccs/Mid1tm1Hzo/Y Tg(EIIa-cre)C5379Lmgd/? (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 04/16/2024 MGI 6.23 |
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