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Symbol
Name
ID
Trpm6
transient receptor potential cation channel, subfamily M, member 6
MGI:2675603
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Seizure
Disease(s) Associated with TRPM6
intestinal hypomagnesemia 1

Mouse Phenotypes
abnormal neural tube closure
spina bifida occulta
abnormal brain development
exencephaly
Availability Mouse Genotype
Trpm6tm1.1Rws/Trpm6tm1.1Rws

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
05/21/2024
MGI 6.23
The Jackson Laboratory