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Symbol
Name
ID

Dkc1
dyskeratosis congenita 1, dyskerin
MGI:1861727

Phenotype annotations related to respiratory system

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	Tracheoesophageal fistula	Recurrent respiratory infections	Pulmonary fibrosis	Abnormality of the pharynx	Restrictive ventilatory defect
dyskeratosis congenita
X-linked dyskeratosis congenita

Mouse Phenotypes		lung inflammation	increased lung carcinoma incidence	abnormal lung morphology	pulmonary interstitial fibrosis	abnormal pulmonary alveolus morphology	abnormal pulmonary alveolus wall morphology	abnormal pulmonary alveolar parenchyma morphology
Availability	Mouse Genotype	lung inflammation	increased lung carcinoma incidence	abnormal lung morphology	pulmonary interstitial fibrosis	abnormal pulmonary alveolus morphology	abnormal pulmonary alveolus wall morphology	abnormal pulmonary alveolar parenchyma morphology
	Dkc1^tm1Ppp/Dkc1⁺
	Dkc1^tm1Ppp/Y

Contributing Projects: 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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