About Help FAQ

Symbol
Name
ID

Mks1
MKS transition zone complex subunit 1
MGI:3584243

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Large placenta	Single umbilical artery	Oligohydramnios
Disease(s) Associated with MKS1
Meckel syndrome 1

Mouse Phenotypes		abnormal motile primary cilium morphology	decreased embryonic cilium length	decreased embryonic cilium number	absent nodal flow	abnormal embryo turning	abnormal neural tube morphology	abnormal floor plate morphology	incomplete rostral neuropore closure
Availability	Mouse Genotype	abnormal motile primary cilium morphology	decreased embryonic cilium length	decreased embryonic cilium number	absent nodal flow	abnormal embryo turning	abnormal neural tube morphology	abnormal floor plate morphology	incomplete rostral neuropore closure
	Mks1^hlb614/Mks1^hlb614
	Mks1^krc/Mks1^krc
	Mks1^{tm1a(EUCOMM)Wtsi}/Mks1^{tm1a(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/21/2024 MGI 6.23