Symbol Name ID |
Rtel1
regulator of telomere elongation helicase 1 MGI:2139369 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Decreased circulating antibody level |
Disease(s) Associated with RTEL1 | |
autosomal recessive dyskeratosis congenita 5 |
Mouse Phenotypes | cellular phenotype |
abnormal telomere morphology |
abnormal cell physiology |
abnormal mitosis |
abnormal cell differentiation |
early cellular replicative senescence |
decreased DNA replication |
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Availability | Mouse Genotype | |||||||
Rtel1tm1Pml/Rtel1tm1Pml | ||||||||
Rtel1tm2.1Hdin/Rtel1tm2.1Hdin | * | |||||||
Rtel1tm3.1Hdin/Rtel1tm3.1Hdin | * | |||||||
Rtel1tm1Hdin/Rtel1tm1Hdin (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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