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Symbol
Name
ID
Tmem216
transmembrane protein 216
MGI:1920020
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Cystic hygroma
Omphalocele
Failure to thrive
Intrauterine growth retardation
Disease(s) Associated with TMEM216
Joubert syndrome 2
Meckel syndrome 2

Mouse Phenotypes
cleft palate
omphalocele
polycystic kidney
prenatal growth retardation
Availability Mouse Genotype
Tmem216em1Cya/Tmem216em1Cya

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
04/23/2024
MGI 6.23
The Jackson Laboratory