Symbol Name ID |
Mks1
MKS transition zone complex subunit 1 MGI:3584243 |
Darker colors indicate more annotations |
Human Phenotypes | Short neck |
Webbed neck |
Splenomegaly |
Omphalocele |
Short stature |
Obesity |
Childhood-onset truncal obesity |
Intrauterine growth retardation |
Disease(s) Associated with MKS1 | ||||||||
Bardet-Biedl syndrome | ||||||||
Bardet-Biedl syndrome 13 | ||||||||
Meckel syndrome 1 |
Mouse Phenotypes | enlarged heart |
cleft upper lip |
cleft palate |
pointed snout |
omphalocele |
kidney cyst |
kidney cortex cyst |
polycystic kidney |
liver cyst |
heterotaxia |
left pulmonary isomerism |
situs inversus |
enlarged kidney |
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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 03/19/2024 MGI 6.23 |
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