Symbol Name ID |
Dkc1
dyskeratosis congenita 1, dyskerin MGI:1861727 |
Darker colors indicate more annotations |
Human Phenotypes | Tracheoesophageal fistula |
Recurrent respiratory infections |
Pulmonary fibrosis |
Abnormality of the pharynx |
Restrictive ventilatory defect |
Disease(s) Associated with DKC1 | |||||
dyskeratosis congenita | |||||
X-linked dyskeratosis congenita |
Mouse Phenotypes | lung inflammation |
increased lung carcinoma incidence |
abnormal lung morphology |
pulmonary interstitial fibrosis |
abnormal pulmonary alveolus morphology |
increased pulmonary alveolus wall thickness |
abnormal pulmonary alveolar parenchyma morphology |
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Availability | Mouse Genotype | |||||||
Dkc1tm1Ppp/Dkc1+ | ||||||||
Dkc1tm1Ppp/Y |
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 09/03/2024 MGI 6.24 |
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