Symbol Name ID |
Kcnq1ot1
KCNQ1 overlapping transcript 1 MGI:1926855 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | cellular phenotype |
abnormal DNA methylation |
abnormal imprinting |
maternal imprinting |
genetic imprinting |
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Availability | Mouse Genotype | |||||
Kcnq1ot1tm1.1Ckan/Kcnq1ot1tm1.1Ckan | * | |||||
Kcnq1ot1tm1.1Ckan/Kcnq1ot1+ | ||||||
Kcnq1ot1tm1.1Mjh/Kcnq1ot1+ | ||||||
Kcnq1ot1tm1Tilg/Kcnq1ot1+ | ||||||
Kcnq1ot1tm2Mjh/Kcnq1ot1+ | ||||||
Kcnq1ot1tm2Tilg/Kcnq1ot1+ | ||||||
Kcnq1ot1tm3Mjh/Kcnq1ot1+ | ||||||
Kcnq1ot1tm3Tilg/Kcnq1ot1+ | ||||||
Kcnq1ot1tm4Tilg/Kcnq1ot1+ | ||||||
Kcnq1ot1tm2.1Ckan/Kcnq1ot1+ Meox2tm1(cre)Sor/Meox2+ (conditional) |
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Kcnq1ot1tm2.1Ckan/Kcnq1ot1+ Tg(CAG-cre/Esr1*)5Amc/0 (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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