Symbol Name ID |
Clxn
calaxin MGI:1914043 |
Darker colors indicate more annotations |
Human Phenotypes | Chronic sinusitis |
Anomalous pulmonary venous return |
Recurrent sinopulmonary infections |
Wheezing |
Pulmonary situs ambiguus |
Peribronchovascular interstitial thickening |
Respiratory tract infection |
Atelectasis |
Abnormal sputum |
Lithoptysis |
Bronchiectasis |
Airway obstruction |
Productive cough |
Neonatal respiratory distress |
Respiratory failure |
Disease(s) Associated with CLXN | |||||||||||||||
primary ciliary dyskinesia |
Mouse Phenotypes | abnormal respiratory motile cilium physiology |
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Availability | Mouse Genotype | |
Clxntm1.1Osb/Clxntm1.1Osb |
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 08/02/2024 MGI 6.24 |
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