Symbol Name ID |
Tmem216
transmembrane protein 216 MGI:1920020 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Biparietal narrowing |
Dolichocephaly |
Dandy-Walker malformation |
Macrocephaly |
Metopic synostosis |
Encephalocele |
Bowing of the long bones |
Postaxial hand polydactyly |
Hand polydactyly |
Postaxial foot polydactyly |
Foot polydactyly |
Polydactyly |
Scoliosis |
Abnormal form of the vertebral bodies |
Disease(s) Associated with TMEM216 | |||||||||||||||
Joubert syndrome | |||||||||||||||
Joubert syndrome 2 | |||||||||||||||
Meckel syndrome 2 |
Mouse Phenotypes | micrognathia |
split sternum |
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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 05/14/2024 MGI 6.23 |
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