Symbol Name ID |
Mks1
MKS transition zone complex subunit 1 MGI:3584243 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Asthma |
Pulmonary hypoplasia |
Abnormality of the larynx |
Disease(s) Associated with MKS1 | |||
Bardet-Biedl syndrome | |||
Meckel syndrome 1 |
Mouse Phenotypes | respiratory system phenotype |
left pulmonary isomerism |
fused right lung lobes |
pulmonary hypoplasia |
decreased respiration |
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Availability | Mouse Genotype | |||||
Mks1hlb614/Mks1hlb614 | * | |||||
Mks1krc/Mks1krc | ||||||
Mks1tm1a(EUCOMM)Wtsi/Mks1tm1a(EUCOMM)Wtsi |
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 04/23/2024 MGI 6.23 |
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