Symbol Name ID |
Tmem216
transmembrane protein 216 MGI:1920020 |
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 |
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Availability | Mouse Genotype | ||||
Tmem216em1Cya/Tmem216em1Cya |
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 |
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