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Symbol Name ID |
Gcm2
glial cells missing homolog 2 MGI:1861438 |
| Darker colors indicate more annotations |
| Human Phenotypes | Chondrocalcinosis |
Osteopenia |
Generalized osteoporosis |
Cerebral calcification |
| Disease(s) Associated with GCM2 | ||||
| familial isolated hypoparathyroidism | ||||
| hyperparathyroidism |
| Mouse Phenotypes | abnormal trabecular bone morphology |
increased bone mass |
abnormal bone ossification |
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| Availability | Mouse Genotype | |||
| Gcm2tm1Kry/Gcm2tm1Kry | ||||
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 04/09/2024 MGI 6.23 |
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