|
Symbol Name ID |
Tbce
tubulin-specific chaperone E MGI:1917680 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Decreased response to growth hormone stimulation test |
Delayed myelination |
Ventriculomegaly |
Hypoplasia of the corpus callosum |
Intellectual disability |
Hypocalcemic tetany |
Seizure |
Hypocalcemic seizures |
| Disease(s) Associated with TBCE | |||||||||
| hypoparathyroidism-retardation-dysmorphism syndrome | |||||||||
| Kenny-Caffey syndrome type 1 |
| Mouse Phenotypes | motor neuron degeneration |
abnormal facial nerve morphology |
abnormal phrenic nerve morphology |
axon degeneration |
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| Availability | Mouse Genotype | ||||
| Tbcepmn/Tbcepmn | |||||
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 07/08/2026 MGI 6.24 |
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