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Symbol Name ID |
Tmem138
transmembrane protein 138 MGI:1920232 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Encephalocele |
Polydactyly |
| Disease(s) Associated with TMEM138 | |||
| Joubert syndrome 16 |
| Mouse Phenotypes | decreased bone mineral content |
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| Availability | Mouse Genotype | |
| Tmem138tm1b(EUCOMM)Wtsi/Tmem138tm1b(EUCOMM)Wtsi | ||
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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