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Symbol
Name
ID
Mks1
MKS transition zone complex subunit 1
MGI:3584243
Phenotype annotations related to growth/size/body
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
Availability Mouse Genotype
Mks1hlb614/Mks1hlb614
Mks1krc/Mks1krc
Mks1tm1a(EUCOMM)Wtsi/Mks1tm1a(EUCOMM)Wtsi

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)
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last database update
03/19/2024
MGI 6.23
The Jackson Laboratory