Symbol Name ID |
Nme5
NME/NM23 family member 5 MGI:1922783 |
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 NME5 | |||||||||||||||
primary ciliary dyskinesia |
Mouse Phenotypes | nasal inflammation |
maxillary sinus inflammation |
impaired mucociliary clearance |
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Availability | Mouse Genotype | |||
Nme5tm1Lex/Nme5tm1Lex |
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 05/14/2024 MGI 6.23 |
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