Symbol Name ID |
Orc1
origin recognition complex, subunit 1 MGI:1328337 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with ORC1 | |
Meier-Gorlin syndrome 1 |
Mouse Phenotypes | embryonic lethality prior to organogenesis |
embryonic lethality at implantation, complete penetrance |
embryonic lethality, complete penetrance |
prenatal lethality prior to heart atrial septation |
preweaning lethality, complete penetrance |
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Availability | Mouse Genotype | |||||
Orc1tm1.2Gle/Orc1tm1.2Gle | ||||||
Orc1tm1a(KOMP)Wtsi/Orc1tm1a(KOMP)Wtsi | ||||||
Orc1tm1b(KOMP)Wtsi/Orc1tm1b(KOMP)Wtsi | ||||||
Orc1tm1.1Gle/Orc1tm1.2Gle Edil3Tg(Sox2-cre)1Amc/Edil3+ (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 04/16/2024 MGI 6.23 |
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