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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 04/16/2024 MGI 6.23 |
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