|
Symbol Name ID |
Flna
filamin, alpha MGI:95556 |
| Darker colors indicate more annotations |
| Human Phenotypes | Absent frontal sinuses |
Hypoplastic frontal sinuses |
Pulmonary arterial hypertension |
Recurrent respiratory infections |
Stridor |
Dyspnea |
Pulmonary hypoplasia |
Respiratory insufficiency |
Respiratory failure |
| Disease(s) Associated with FLNA | |||||||||
| frontometaphyseal dysplasia 1 | |||||||||
| Melnick-Needles syndrome | |||||||||
| otopalatodigital syndrome type 1 | |||||||||
| otopalatodigital syndrome type 2 | |||||||||
| X-linked cardiac valvular dysplasia |
| Mouse Phenotypes | emphysema |
|
| Availability | Mouse Genotype | |
| Flnatm1.2Caw/Flna+ | ||
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 05/21/2024 MGI 6.23 |
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