About   Help   FAQ
Symbol
Name
ID
Fbln5
fibulin 5
MGI:1346091
Phenotype annotations related to respiratory system
Darker colors indicate more annotations
Human Phenotypes
Peripheral pulmonary artery stenosis
Recurrent respiratory infections
Emphysema
Disease(s) Associated with FBLN5
autosomal recessive cutis laxa type IA

Mouse Phenotypes
abnormal pulmonary circulation
abnormal lung morphology
abnormal pulmonary alveolus morphology
emphysema
abnormal terminal bronchiole morphology
Availability Mouse Genotype
Fbln5tm1Eno/Fbln5tm1Eno
Fbln5tm1Krc/Fbln5tm1Krc

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory